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rs1085307599

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position70035364
GeneEDA
is asnp
is mentioned by
dbSNPrs1085307599
dbSNP (old)rs1085307599
ClinGenrs1085307599
ebirs1085307599
HLIrs1085307599
Exacrs1085307599
Gnomadrs1085307599
Varsomers1085307599
Maprs1085307599
PheGenIrs1085307599
Biobankrs1085307599
1000 genomesrs1085307599
hgdprs1085307599
ensemblrs1085307599
gopubmedrs1085307599
geneviewrs1085307599
scholarrs1085307599
googlers1085307599
pharmgkbrs1085307599
gwascentralrs1085307599
openSNPrs1085307599
23andMers1085307599
23andMe allrs1085307599
SNPshotrs1085307599
SNPdbers1085307599
MSV3drs1085307599
GWAS Ctlgrs1085307599
Max Magnitude0
ClinVar
Risk rs1085307599(C;C)
Alt rs1085307599(C;C)
Reference Rs1085307599(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EDA
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.69255214T>C
CLNSRC
CLNACC RCV000489664.1,