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rs1064793105

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position70030491
GeneEDA
is asnp
is mentioned by
dbSNPrs1064793105
dbSNP (old)rs1064793105
ClinGenrs1064793105
ebirs1064793105
HLIrs1064793105
Exacrs1064793105
Gnomadrs1064793105
Varsomers1064793105
LitVarrs1064793105
Maprs1064793105
PheGenIrs1064793105
Biobankrs1064793105
1000 genomesrs1064793105
hgdprs1064793105
ensemblrs1064793105
gopubmedrs1064793105
geneviewrs1064793105
scholarrs1064793105
googlers1064793105
pharmgkbrs1064793105
gwascentralrs1064793105
openSNPrs1064793105
23andMers1064793105
23andMe allrs1064793105
SNPshotrs1064793105
SNPdbers1064793105
MSV3drs1064793105
GWAS Ctlgrs1064793105
Max Magnitude0
ClinVar
Risk rs1064793105(A;A)
Alt rs1064793105(A;A)
Reference Rs1064793105(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EDA
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.69250341G>A
CLNSRC
CLNACC RCV000480945.1,