SLC9A3

solute carrier family 9 member A3
OMIM: 182307, ClinGen, DECIPHER

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green SLC9A3 in Congenital Diarrhoea Level 2: Gastroenterological disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Diarrhoea 8, secretory sodium, congenital 616868
Amber SLC9A3 in Inflammatory bowel disease Level 2: Gastroenterological disorders Version 1.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert Review Phenotypes Diarrhoea 8, secretory sodium, congenital 616868 Very Early Onset Inflammatory Bowel Disease
Green SLC9A3 in Mendeliome Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Diarrhoea 8, secretory sodium, congenital 616868
Green SLC9A3 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 1.0	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Diarrhea 8, secretory sodium, congenital, 616868 (3), Autosomal recessive
Amber SLC9A3 in Prepair 1000+ Level 2: Screening Version 3.0	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Mackenzie's Mission Phenotypes Diarrhea 8, secretory sodium, congenital, 616868 (3), Autosomal recessive
Amber SLC9A3 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 2.0	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Diarrhoea 8, secretory sodium, congenital, MiM# 616868 Tags for review