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rs63750904

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
(I;I) 0
(TG;TG) 0 common in clinvar
Make rs63750904(-;-)
Make rs63750904(-;GT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47800702
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750904
ebirs63750904
HLIrs63750904
Exacrs63750904
Varsomers63750904
Maprs63750904
PheGenIrs63750904
hapmaprs63750904
1000 genomesrs63750904
hgdprs63750904
ensemblrs63750904
gopubmedrs63750904
geneviewrs63750904
scholarrs63750904
googlers63750904
pharmgkbrs63750904
gwascentralrs63750904
openSNPrs63750904
23andMers63750904
23andMe allrs63750904
SNP Nexus

SNPshotrs63750904
SNPdbers63750904
MSV3drs63750904
GWAS Ctlgrs63750904
Max Magnitude0
ClinVar
Risk rs63750904(;)
Alt rs63750904(;)
Reference rs63750904(TG;TG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027841_48027842delGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074776.2,