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rs1085307918

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome11
Position64758670
GenePYGM
is asnp
is mentioned by
dbSNPrs1085307918
dbSNP (old)rs1085307918
ClinGenrs1085307918
ebirs1085307918
HLIrs1085307918
Exacrs1085307918
Gnomadrs1085307918
Varsomers1085307918
Maprs1085307918
PheGenIrs1085307918
Biobankrs1085307918
1000 genomesrs1085307918
hgdprs1085307918
ensemblrs1085307918
gopubmedrs1085307918
geneviewrs1085307918
scholarrs1085307918
googlers1085307918
pharmgkbrs1085307918
gwascentralrs1085307918
openSNPrs1085307918
23andMers1085307918
23andMe allrs1085307918
SNPshotrs1085307918
SNPdbers1085307918
MSV3drs1085307918
GWAS Ctlgrs1085307918
Max Magnitude0
ClinVar
Risk rs1085307918(T;T)
Alt rs1085307918(T;T)
Reference Rs1085307918(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PYGM
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64526142C>A
CLNSRC
CLNACC RCV000489939.1,