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rs1064793106

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position70033527
GeneEDA
is asnp
is mentioned by
dbSNPrs1064793106
dbSNP (old)rs1064793106
ClinGenrs1064793106
ebirs1064793106
HLIrs1064793106
Exacrs1064793106
Gnomadrs1064793106
Varsomers1064793106
Maprs1064793106
PheGenIrs1064793106
Biobankrs1064793106
1000 genomesrs1064793106
hgdprs1064793106
ensemblrs1064793106
gopubmedrs1064793106
geneviewrs1064793106
scholarrs1064793106
googlers1064793106
pharmgkbrs1064793106
gwascentralrs1064793106
openSNPrs1064793106
23andMers1064793106
23andMe allrs1064793106
SNPshotrs1064793106
SNPdbers1064793106
MSV3drs1064793106
GWAS Ctlgrs1064793106
Max Magnitude0
ClinVar
Risk rs1064793106(G;G)
Alt rs1064793106(G;G)
Reference Rs1064793106(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EDA
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.69253377A>G
CLNSRC
CLNACC RCV000483933.1,