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rs786202848

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202848(A;A)
Make rs786202848(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47798972
GeneMSH6
is asnp
is mentioned by
dbSNPrs786202848
ebirs786202848
HLIrs786202848
Exacrs786202848
Varsomers786202848
Maprs786202848
PheGenIrs786202848
hapmaprs786202848
1000 genomesrs786202848
hgdprs786202848
ensemblrs786202848
gopubmedrs786202848
geneviewrs786202848
scholarrs786202848
googlers786202848
pharmgkbrs786202848
gwascentralrs786202848
openSNPrs786202848
23andMers786202848
23andMe allrs786202848
SNP Nexus

SNPshotrs786202848
SNPdbers786202848
MSV3drs786202848
GWAS Ctlgrs786202848
Max Magnitude0
ClinVar
Risk rs786202848(A;A)
Alt rs786202848(A;A)
Reference rs786202848(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026111C>A
CLNSRC
CLNACC RCV000165878.1, RCV000233544.1,