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rs1085307678

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position48685763
GeneWAS
is asnp
is mentioned by
dbSNPrs1085307678
dbSNP (classic)rs1085307678
ClinGenrs1085307678
ebirs1085307678
HLIrs1085307678
Exacrs1085307678
Gnomadrs1085307678
Varsomers1085307678
LitVarrs1085307678
Maprs1085307678
PheGenIrs1085307678
Biobankrs1085307678
1000 genomesrs1085307678
hgdprs1085307678
ensemblrs1085307678
geneviewrs1085307678
scholarrs1085307678
googlers1085307678
pharmgkbrs1085307678
gwascentralrs1085307678
openSNPrs1085307678
23andMers1085307678
SNPshotrs1085307678
SNPdbers1085307678
MSV3drs1085307678
GWAS Ctlgrs1085307678
Max Magnitude0
ClinVar
Risk rs1085307678(-;-)
Alt rs1085307678(-;-)
Reference Rs1085307678(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene WAS
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.48544152delC
CLNSRC
CLNACC RCV000489103.1,