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rs374230313

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374230313(C;T)
Make rs374230313(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800533
GeneMSH6
is asnp
is mentioned by
dbSNPrs374230313
ebirs374230313
HLIrs374230313
Exacrs374230313
Varsomers374230313
Maprs374230313
PheGenIrs374230313
hapmaprs374230313
1000 genomesrs374230313
hgdprs374230313
ensemblrs374230313
gopubmedrs374230313
geneviewrs374230313
scholarrs374230313
googlers374230313
pharmgkbrs374230313
gwascentralrs374230313
openSNPrs374230313
23andMers374230313
23andMe allrs374230313
SNP Nexus

SNPshotrs374230313
SNPdbers374230313
MSV3drs374230313
GWAS Ctlgrs374230313
Max Magnitude0
ClinVar
Risk rs374230313(A,T;A,T)
Alt rs374230313(A,T;A,T)
Reference rs374230313(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48027672C>A
CLNSRC
CLNACC RCV000166285.1,