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rs1085308021

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome11
Position64758464
GenePYGM
is asnp
is mentioned by
dbSNPrs1085308021
dbSNP (old)rs1085308021
ClinGenrs1085308021
ebirs1085308021
HLIrs1085308021
Exacrs1085308021
Gnomadrs1085308021
Varsomers1085308021
Maprs1085308021
PheGenIrs1085308021
Biobankrs1085308021
1000 genomesrs1085308021
hgdprs1085308021
ensemblrs1085308021
gopubmedrs1085308021
geneviewrs1085308021
scholarrs1085308021
googlers1085308021
pharmgkbrs1085308021
gwascentralrs1085308021
openSNPrs1085308021
23andMers1085308021
23andMe allrs1085308021
SNPshotrs1085308021
SNPdbers1085308021
MSV3drs1085308021
GWAS Ctlgrs1085308021
Max Magnitude0
ClinVar
Risk rs1085308021(A;A)
Alt rs1085308021(A;A)
Reference Rs1085308021(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PYGM
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64525936C>T
CLNSRC
CLNACC RCV000489796.1,