SLC9A1, solute carrier family 9 member A1, 6548

N. diseases: 144; N. variants: 4
Disease: LICHTENSTEIN-KNORR SYNDROME ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786204831
rs786204831
Entrez Id: 6548
Gene Symbol: SLC9A1
SLC9A1
CUI: C4225383
Disease:
LICHTENSTEIN-KNORR SYNDROME 		0.800 GeneticVariation UNIPROT
dbSNP: rs786204831
rs786204831
Entrez Id: 6548
Gene Symbol: SLC9A1
SLC9A1
CUI: C4225383
Disease:
LICHTENSTEIN-KNORR SYNDROME 		T 0.800 CausalMutation CLINVAR