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rs63750924

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs63750924(-;-)
Make rs63750924(-;TC)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410114
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750924
ebirs63750924
HLIrs63750924
Exacrs63750924
Varsomers63750924
Maprs63750924
PheGenIrs63750924
hapmaprs63750924
1000 genomesrs63750924
hgdprs63750924
ensemblrs63750924
gopubmedrs63750924
geneviewrs63750924
scholarrs63750924
googlers63750924
pharmgkbrs63750924
gwascentralrs63750924
openSNPrs63750924
23andMers63750924
23andMe allrs63750924
SNP Nexus

SNPshotrs63750924
SNPdbers63750924
MSV3drs63750924
GWAS Ctlgrs63750924
Max Magnitude0
ClinVar
Risk rs63750924(;)
Alt rs63750924(;)
Reference rs63750924(TC;TC)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47637253_47637254delTC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076591.3, RCV000202145.2,