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rs63751622

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs63751622(-;-)
Make rs63751622(-;TG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410365
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751622
ebirs63751622
HLIrs63751622
Exacrs63751622
Varsomers63751622
Maprs63751622
PheGenIrs63751622
hapmaprs63751622
1000 genomesrs63751622
hgdprs63751622
ensemblrs63751622
gopubmedrs63751622
geneviewrs63751622
scholarrs63751622
googlers63751622
pharmgkbrs63751622
gwascentralrs63751622
openSNPrs63751622
23andMers63751622
23andMe allrs63751622
SNP Nexus

SNPshotrs63751622
SNPdbers63751622
MSV3drs63751622
GWAS Ctlgrs63751622
Max Magnitude0
ClinVar
Risk rs63751622(;)
Alt rs63751622(;)
Reference rs63751622(TG;TG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637504_47637505delTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076656.2,