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rs1060502001

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502001(A;T)
Make rs1060502001(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47403276
GeneMSH2
is asnp
is mentioned by
dbSNPrs1060502001
dbSNP (old)rs1060502001
ClinGenrs1060502001
ebirs1060502001
HLIrs1060502001
Exacrs1060502001
Gnomadrs1060502001
Varsomers1060502001
Maprs1060502001
PheGenIrs1060502001
Biobankrs1060502001
1000 genomesrs1060502001
hgdprs1060502001
ensemblrs1060502001
gopubmedrs1060502001
geneviewrs1060502001
scholarrs1060502001
googlers1060502001
pharmgkbrs1060502001
gwascentralrs1060502001
openSNPrs1060502001
23andMers1060502001
23andMe allrs1060502001
SNPshotrs1060502001
SNPdbers1060502001
MSV3drs1060502001
GWAS Ctlgrs1060502001
Max Magnitude0
ClinVar
Risk rs1060502001(T;T)
Alt rs1060502001(T;T)
Reference Rs1060502001(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630415A>T
CLNSRC
CLNACC RCV000467909.1,