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rs63751227

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs63751227(-;-)
Make rs63751227(-;AT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410107
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751227
ebirs63751227
HLIrs63751227
Exacrs63751227
Varsomers63751227
Maprs63751227
PheGenIrs63751227
hapmaprs63751227
1000 genomesrs63751227
hgdprs63751227
ensemblrs63751227
gopubmedrs63751227
geneviewrs63751227
scholarrs63751227
googlers63751227
pharmgkbrs63751227
gwascentralrs63751227
openSNPrs63751227
23andMers63751227
23andMe allrs63751227
SNP Nexus

SNPshotrs63751227
SNPdbers63751227
MSV3drs63751227
GWAS Ctlgrs63751227
Max Magnitude0
ClinVar
Risk rs63751227(;)
Alt rs63751227(;)
Reference rs63751227(AT;AT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637246_47637247delAT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076590.2,