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rs1064795546

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome1
Position21881369
GeneHSPG2
is asnp
is mentioned by
dbSNPrs1064795546
dbSNP (old)rs1064795546
ClinGenrs1064795546
ebirs1064795546
HLIrs1064795546
Exacrs1064795546
Gnomadrs1064795546
Varsomers1064795546
Maprs1064795546
PheGenIrs1064795546
Biobankrs1064795546
1000 genomesrs1064795546
hgdprs1064795546
ensemblrs1064795546
gopubmedrs1064795546
geneviewrs1064795546
scholarrs1064795546
googlers1064795546
pharmgkbrs1064795546
gwascentralrs1064795546
openSNPrs1064795546
23andMers1064795546
23andMe allrs1064795546
SNPshotrs1064795546
SNPdbers1064795546
MSV3drs1064795546
GWAS Ctlgrs1064795546
Max Magnitude0
ClinVar
Risk rs1064795546(A;A)
Alt rs1064795546(A;A)
Reference Rs1064795546(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HSPG2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.22207862C>T
CLNSRC
CLNACC RCV000483256.1,