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rs1064795077

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome7
Position76303853
GeneHSPB1
is asnp
is mentioned by
dbSNPrs1064795077
dbSNP (old)rs1064795077
ClinGenrs1064795077
ebirs1064795077
HLIrs1064795077
Exacrs1064795077
Gnomadrs1064795077
Varsomers1064795077
Maprs1064795077
PheGenIrs1064795077
Biobankrs1064795077
1000 genomesrs1064795077
hgdprs1064795077
ensemblrs1064795077
gopubmedrs1064795077
geneviewrs1064795077
scholarrs1064795077
googlers1064795077
pharmgkbrs1064795077
gwascentralrs1064795077
openSNPrs1064795077
23andMers1064795077
23andMe allrs1064795077
SNPshotrs1064795077
SNPdbers1064795077
MSV3drs1064795077
GWAS Ctlgrs1064795077
Max Magnitude0
ClinVar
Risk rs1064795077(T;T)
Alt rs1064795077(T;T)
Reference Rs1064795077(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HSPB1
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.75933170C>T
CLNSRC
CLNACC RCV000486834.1,