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rs1060505055

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060505055(G;T)
Make rs1060505055(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position31759476
GeneMSH5, MSH5-SAPCD1
is asnp
is mentioned by
dbSNPrs1060505055
dbSNP (classic)rs1060505055
ClinGenrs1060505055
ebirs1060505055
HLIrs1060505055
Exacrs1060505055
Gnomadrs1060505055
Varsomers1060505055
LitVarrs1060505055
Maprs1060505055
PheGenIrs1060505055
Biobankrs1060505055
1000 genomesrs1060505055
hgdprs1060505055
ensemblrs1060505055
geneviewrs1060505055
scholarrs1060505055
googlers1060505055
pharmgkbrs1060505055
gwascentralrs1060505055
openSNPrs1060505055
23andMers1060505055
23andMe allrs1060505055
SNPshotrs1060505055
SNPdbers1060505055
MSV3drs1060505055
GWAS Ctlgrs1060505055
Max Magnitude0
ClinVar
Risk rs1060505055(T;T)
Alt rs1060505055(T;T)
Reference Rs1060505055(G;G)
Significance Pathogenic
Disease Premature ovarian failure 13
Variation info
Gene MSH5-SAPCD1 MSH5
CLNDBN Premature ovarian failure 13
Reversed 0
HGVS NC_000006.11:g.31727253G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000477966.1,