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rs63751036

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
(TA;TA) 0 common in clinvar
Make rs63751036(-;-)
Make rs63751036(-;TA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478301
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751036
ebirs63751036
HLIrs63751036
Exacrs63751036
Varsomers63751036
Maprs63751036
PheGenIrs63751036
hapmaprs63751036
1000 genomesrs63751036
hgdprs63751036
ensemblrs63751036
gopubmedrs63751036
geneviewrs63751036
scholarrs63751036
googlers63751036
pharmgkbrs63751036
gwascentralrs63751036
openSNPrs63751036
23andMers63751036
23andMe allrs63751036
SNP Nexus

SNPshotrs63751036
SNPdbers63751036
MSV3drs63751036
GWAS Ctlgrs63751036
Max Magnitude0
ClinVar
Risk rs63751036(;)
Alt rs63751036(;)
Reference rs63751036(AT;AT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705440_47705441delTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076442.2,