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rs863224482

From SNPedia

Orientationplus
Make rs863224482(-;-)
Make rs863224482(-;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47410146
GeneMSH2
is asnp
is mentioned by
dbSNPrs863224482
ebirs863224482
HLIrs863224482
Exacrs863224482
Varsomers863224482
Maprs863224482
PheGenIrs863224482
hapmaprs863224482
1000 genomesrs863224482
hgdprs863224482
ensemblrs863224482
gopubmedrs863224482
geneviewrs863224482
scholarrs863224482
googlers863224482
pharmgkbrs863224482
gwascentralrs863224482
openSNPrs863224482
23andMers863224482
23andMe allrs863224482
SNP Nexus

SNPshotrs863224482
SNPdbers863224482
MSV3drs863224482
GWAS Ctlgrs863224482
Max Magnitude
ClinVar
Risk rs863224482(;)
Alt rs863224482(;)
Reference rs863224482(AT;AT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637287_47637288delAT
CLNSRC
CLNACC RCV000205179.2,