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rs606231284

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231284(A;A)
Make rs606231284(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position38290229
GeneSPINT2
is asnp
is mentioned by
dbSNPrs606231284
ebirs606231284
HLIrs606231284
Exacrs606231284
Varsomers606231284
Maprs606231284
PheGenIrs606231284
hapmaprs606231284
1000 genomesrs606231284
hgdprs606231284
ensemblrs606231284
gopubmedrs606231284
geneviewrs606231284
scholarrs606231284
googlers606231284
pharmgkbrs606231284
gwascentralrs606231284
openSNPrs606231284
23andMers606231284
23andMe allrs606231284
SNP Nexus

SNPshotrs606231284
SNPdbers606231284
MSV3drs606231284
GWAS Ctlgrs606231284
Max Magnitude0
ClinVar
Risk rs606231284(A;A)
Alt rs606231284(A;A)
Reference rs606231284(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.38780869G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144940.3,