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rs587779179

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779179(-;-)
Make rs587779179(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47412529
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779179
ebirs587779179
HLIrs587779179
Exacrs587779179
Varsomers587779179
Maprs587779179
PheGenIrs587779179
hapmaprs587779179
1000 genomesrs587779179
hgdprs587779179
ensemblrs587779179
gopubmedrs587779179
geneviewrs587779179
scholarrs587779179
googlers587779179
pharmgkbrs587779179
gwascentralrs587779179
openSNPrs587779179
23andMers587779179
23andMe allrs587779179
SNP Nexus

SNPshotrs587779179
SNPdbers587779179
MSV3drs587779179
GWAS Ctlgrs587779179
Max Magnitude0
ClinVar
Risk rs587779179(;)
Alt rs587779179(;)
Reference rs587779179(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639668delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076703.2,