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rs397515875

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515875(C;C)
Make rs397515875(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47803419
GeneMSH6
is asnp
is mentioned by
dbSNPrs397515875
ebirs397515875
HLIrs397515875
Exacrs397515875
Varsomers397515875
Maprs397515875
PheGenIrs397515875
hapmaprs397515875
1000 genomesrs397515875
hgdprs397515875
ensemblrs397515875
gopubmedrs397515875
geneviewrs397515875
scholarrs397515875
googlers397515875
pharmgkbrs397515875
gwascentralrs397515875
openSNPrs397515875
23andMers397515875
23andMe allrs397515875
SNP Nexus

SNPshotrs397515875
SNPdbers397515875
MSV3drs397515875
GWAS Ctlgrs397515875
Max Magnitude0
ClinVar
Risk rs397515875(C;C)
Alt rs397515875(C;C)
Reference rs397515875(G;G)
Significance Other
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48030558G>C
CLNSRC ClinVar GeneDx
CLNACC RCV000035322.2, RCV000115404.4, RCV000201971.1,