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rs1085308006

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position149496419
GeneIDS
is asnp
is mentioned by
dbSNPrs1085308006
dbSNP (old)rs1085308006
ClinGenrs1085308006
ebirs1085308006
HLIrs1085308006
Exacrs1085308006
Gnomadrs1085308006
Varsomers1085308006
Maprs1085308006
PheGenIrs1085308006
Biobankrs1085308006
1000 genomesrs1085308006
hgdprs1085308006
ensemblrs1085308006
gopubmedrs1085308006
geneviewrs1085308006
scholarrs1085308006
googlers1085308006
pharmgkbrs1085308006
gwascentralrs1085308006
openSNPrs1085308006
23andMers1085308006
23andMe allrs1085308006
SNPshotrs1085308006
SNPdbers1085308006
MSV3drs1085308006
GWAS Ctlgrs1085308006
Max Magnitude0
ClinVar
Risk rs1085308006(T;T)
Alt rs1085308006(T;T)
Reference Rs1085308006(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IDS
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.148577950T>A
CLNSRC
CLNACC RCV000489884.1,