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rs1064795749

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome12
Position48130392
GenePFKM
is asnp
is mentioned by
dbSNPrs1064795749
dbSNP (old)rs1064795749
ClinGenrs1064795749
ebirs1064795749
HLIrs1064795749
Exacrs1064795749
Gnomadrs1064795749
Varsomers1064795749
Maprs1064795749
PheGenIrs1064795749
Biobankrs1064795749
1000 genomesrs1064795749
hgdprs1064795749
ensemblrs1064795749
gopubmedrs1064795749
geneviewrs1064795749
scholarrs1064795749
googlers1064795749
pharmgkbrs1064795749
gwascentralrs1064795749
openSNPrs1064795749
23andMers1064795749
23andMe allrs1064795749
SNPshotrs1064795749
SNPdbers1064795749
MSV3drs1064795749
GWAS Ctlgrs1064795749
Max Magnitude0
ClinVar
Risk rs1064795749(T;T)
Alt rs1064795749(T;T)
Reference Rs1064795749(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PFKM
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.48524175C>T
CLNSRC
CLNACC RCV000485301.1,