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rs63750334

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs63750334(-;-)
Make rs63750334(-;GA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403336
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750334
ebirs63750334
HLIrs63750334
Exacrs63750334
Varsomers63750334
Maprs63750334
PheGenIrs63750334
hapmaprs63750334
1000 genomesrs63750334
hgdprs63750334
ensemblrs63750334
gopubmedrs63750334
geneviewrs63750334
scholarrs63750334
googlers63750334
pharmgkbrs63750334
gwascentralrs63750334
openSNPrs63750334
23andMers63750334
23andMe allrs63750334
SNP Nexus

SNPshotrs63750334
SNPdbers63750334
MSV3drs63750334
GWAS Ctlgrs63750334
Max Magnitude0
ClinVar
Risk rs63750334(;)
Alt rs63750334(;)
Reference rs63750334(GA;GA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630475_47630476delGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076168.2,