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rs1064797157

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome11
Position64750585
GenePYGM
is asnp
is mentioned by
dbSNPrs1064797157
dbSNP (old)rs1064797157
ClinGenrs1064797157
ebirs1064797157
HLIrs1064797157
Exacrs1064797157
Gnomadrs1064797157
Varsomers1064797157
Maprs1064797157
PheGenIrs1064797157
Biobankrs1064797157
1000 genomesrs1064797157
hgdprs1064797157
ensemblrs1064797157
gopubmedrs1064797157
geneviewrs1064797157
scholarrs1064797157
googlers1064797157
pharmgkbrs1064797157
gwascentralrs1064797157
openSNPrs1064797157
23andMers1064797157
23andMe allrs1064797157
SNPshotrs1064797157
SNPdbers1064797157
MSV3drs1064797157
GWAS Ctlgrs1064797157
Max Magnitude0
ClinVar
Risk rs1064797157(T;T)
Alt rs1064797157(T;T)
Reference Rs1064797157(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PYGM
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64518057T>A
CLNSRC
CLNACC RCV000488033.1,