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rs63750377

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs63750377(-;-)
Make rs63750377(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47803567
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750377
ebirs63750377
HLIrs63750377
Exacrs63750377
Varsomers63750377
Maprs63750377
PheGenIrs63750377
hapmaprs63750377
1000 genomesrs63750377
hgdprs63750377
ensemblrs63750377
gopubmedrs63750377
geneviewrs63750377
scholarrs63750377
googlers63750377
pharmgkbrs63750377
gwascentralrs63750377
openSNPrs63750377
23andMers63750377
23andMe allrs63750377
SNP Nexus

SNPshotrs63750377
SNPdbers63750377
MSV3drs63750377
GWAS Ctlgrs63750377
Max Magnitude0
ClinVar
Risk rs63750377(;)
Alt rs63750377(;)
Reference rs63750377(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030706delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074839.2,