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rs587779068

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779068(-;-)
Make rs587779068(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47416412
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779068
ebirs587779068
HLIrs587779068
Exacrs587779068
Varsomers587779068
Maprs587779068
PheGenIrs587779068
hapmaprs587779068
1000 genomesrs587779068
hgdprs587779068
ensemblrs587779068
gopubmedrs587779068
geneviewrs587779068
scholarrs587779068
googlers587779068
pharmgkbrs587779068
gwascentralrs587779068
openSNPrs587779068
23andMers587779068
23andMe allrs587779068
SNP Nexus

SNPshotrs587779068
SNPdbers587779068
MSV3drs587779068
GWAS Ctlgrs587779068
Max Magnitude0
ClinVar
Risk rs587779068(;)
Alt rs587779068(;)
Reference rs587779068(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47643551delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076010.2,