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rs63751160

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751160(-;-)
Make rs63751160(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47412527
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751160
ebirs63751160
HLIrs63751160
Exacrs63751160
Varsomers63751160
Maprs63751160
PheGenIrs63751160
hapmaprs63751160
1000 genomesrs63751160
hgdprs63751160
ensemblrs63751160
gopubmedrs63751160
geneviewrs63751160
scholarrs63751160
googlers63751160
pharmgkbrs63751160
gwascentralrs63751160
openSNPrs63751160
23andMers63751160
23andMe allrs63751160
SNP Nexus

SNPshotrs63751160
SNPdbers63751160
MSV3drs63751160
GWAS Ctlgrs63751160
Max Magnitude0
ClinVar
Risk rs63751160(;)
Alt rs63751160(;)
Reference rs63751160(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639666delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076702.2,