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rs63751614

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs63751614(-;-)
Make rs63751614(-;AT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47412556
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751614
ebirs63751614
HLIrs63751614
Exacrs63751614
Varsomers63751614
Maprs63751614
PheGenIrs63751614
hapmaprs63751614
1000 genomesrs63751614
hgdprs63751614
ensemblrs63751614
gopubmedrs63751614
geneviewrs63751614
scholarrs63751614
googlers63751614
pharmgkbrs63751614
gwascentralrs63751614
openSNPrs63751614
23andMers63751614
23andMe allrs63751614
SNP Nexus

SNPshotrs63751614
SNPdbers63751614
MSV3drs63751614
GWAS Ctlgrs63751614
Max Magnitude0
ClinVar
Risk rs63751614(;)
Alt rs63751614(;)
Reference rs63751614(AT;AT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639695_47639696delAT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076708.2,