Have questions? Visit https://www.reddit.com/r/SNPedia

rs727503009

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727503009(A;T)
Make rs727503009(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position70033521
GeneEDA
is asnp
is mentioned by
dbSNPrs727503009
dbSNP (classic)rs727503009
ClinGenrs727503009
ebirs727503009
HLIrs727503009
Exacrs727503009
Gnomadrs727503009
Varsomers727503009
LitVarrs727503009
Maprs727503009
PheGenIrs727503009
Biobankrs727503009
1000 genomesrs727503009
hgdprs727503009
ensemblrs727503009
geneviewrs727503009
scholarrs727503009
googlers727503009
pharmgkbrs727503009
gwascentralrs727503009
openSNPrs727503009
23andMers727503009
SNPshotrs727503009
SNPdbers727503009
MSV3drs727503009
GWAS Ctlgrs727503009
Max Magnitude0
ClinVar
Risk rs727503009(G;G) rs727503009(T;T)
Alt rs727503009(G;G) rs727503009(T;T)
Reference Rs727503009(A;A)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene EDA
CLNDBN not provided not specified
Reversed 0
HGVS NC_000023.10:g.69253371A>G; NC_000023.10:g.69253371A>T
CLNSRC
CLNACC RCV000478625.1, RCV000150604.1,