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rs63751234

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(I;I) 0
Make rs63751234(-;-)
Make rs63751234(-;C)
ReferenceGRCh38 38.1/142
Chromosome2
Position47799585
GeneMSH6
is asnp
is mentioned by
dbSNPrs63751234
ebirs63751234
HLIrs63751234
Exacrs63751234
Varsomers63751234
Maprs63751234
PheGenIrs63751234
hapmaprs63751234
1000 genomesrs63751234
hgdprs63751234
ensemblrs63751234
gopubmedrs63751234
geneviewrs63751234
scholarrs63751234
googlers63751234
pharmgkbrs63751234
gwascentralrs63751234
openSNPrs63751234
23andMers63751234
23andMe allrs63751234
SNP Nexus

SNPshotrs63751234
SNPdbers63751234
MSV3drs63751234
GWAS Ctlgrs63751234
Max Magnitude0


ClinVar
Risk rs63751234(;)
Alt rs63751234(;)
Reference rs63751234(C;C)
Significance Pathogenic
Disease Hereditary nonpolyposis colorectal cancer type 5
Variation info
Gene MSH6
CLNDBN Hereditary nonpolyposis colorectal cancer type 5
Reversed 0
HGVS NC_000002.11:g.48026724delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000009488.3,