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rs63749938

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs63749938(-;-)
Make rs63749938(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47800967
GeneMSH6
is asnp
is mentioned by
dbSNPrs63749938
ebirs63749938
HLIrs63749938
Exacrs63749938
Varsomers63749938
Maprs63749938
PheGenIrs63749938
hapmaprs63749938
1000 genomesrs63749938
hgdprs63749938
ensemblrs63749938
gopubmedrs63749938
geneviewrs63749938
scholarrs63749938
googlers63749938
pharmgkbrs63749938
gwascentralrs63749938
openSNPrs63749938
23andMers63749938
23andMe allrs63749938
SNP Nexus

SNPshotrs63749938
SNPdbers63749938
MSV3drs63749938
GWAS Ctlgrs63749938
Max Magnitude0
ClinVar
Risk rs63749938(;)
Alt rs63749938(;)
Reference rs63749938(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48028106delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074794.2,