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rs786204831

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204831(A;A)
Make rs786204831(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position27109678
GeneSLC9A1
is asnp
is mentioned by
dbSNPrs786204831
ebirs786204831
HLIrs786204831
Exacrs786204831
Varsomers786204831
Maprs786204831
PheGenIrs786204831
hapmaprs786204831
1000 genomesrs786204831
hgdprs786204831
ensemblrs786204831
gopubmedrs786204831
geneviewrs786204831
scholarrs786204831
googlers786204831
pharmgkbrs786204831
gwascentralrs786204831
openSNPrs786204831
23andMers786204831
23andMe allrs786204831
SNP Nexus

SNPshotrs786204831
SNPdbers786204831
MSV3drs786204831
GWAS Ctlgrs786204831
Max Magnitude0
ClinVar
Risk rs786204831(A;A)
Alt rs786204831(A;A)
Reference rs786204831(G;G)
Significance Pathogenic
Disease Lichtenstein-knorr syndrome
Variation info
Gene SLC9A1
CLNDBN Lichtenstein-knorr syndrome
Reversed 1
HGVS NC_000001.10:g.27436169C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000169735.5,