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rs606231154

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231154(A;A)
Make rs606231154(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position38291839
GeneSPINT2
is asnp
is mentioned by
dbSNPrs606231154
ebirs606231154
HLIrs606231154
Exacrs606231154
Varsomers606231154
Maprs606231154
PheGenIrs606231154
hapmaprs606231154
1000 genomesrs606231154
hgdprs606231154
ensemblrs606231154
gopubmedrs606231154
geneviewrs606231154
scholarrs606231154
googlers606231154
pharmgkbrs606231154
gwascentralrs606231154
openSNPrs606231154
23andMers606231154
23andMe allrs606231154
SNP Nexus

SNPshotrs606231154
SNPdbers606231154
MSV3drs606231154
GWAS Ctlgrs606231154
Max Magnitude0
ClinVar
Risk rs606231154(A;A)
Alt rs606231154(A;A)
Reference rs606231154(G;G)
Significance Pathogenic
Disease Diarrhea 3
Variation info
Gene SPINT2
CLNDBN Diarrhea 3, secretory sodium, congenital, syndromic
Reversed 0
HGVS NC_000019.9:g.38782479G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005514.3,