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rs63751621

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs63751621(-;-)
Make rs63751621(-;TG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47480703
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751621
ebirs63751621
HLIrs63751621
Exacrs63751621
Varsomers63751621
Maprs63751621
PheGenIrs63751621
hapmaprs63751621
1000 genomesrs63751621
hgdprs63751621
ensemblrs63751621
gopubmedrs63751621
geneviewrs63751621
scholarrs63751621
googlers63751621
pharmgkbrs63751621
gwascentralrs63751621
openSNPrs63751621
23andMers63751621
23andMe allrs63751621
SNP Nexus

SNPshotrs63751621
SNPdbers63751621
MSV3drs63751621
GWAS Ctlgrs63751621
Max Magnitude0
ClinVar
Risk rs63751621(;)
Alt rs63751621(;)
Reference rs63751621(TG;TG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47707842_47707843delTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076483.2,