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rs727504814

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727504814(G;G)
Make rs727504814(G;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position69616706
GeneEDA
is asnp
is mentioned by
dbSNPrs727504814
ebirs727504814
HLIrs727504814
Exacrs727504814
Varsomers727504814
Maprs727504814
PheGenIrs727504814
hapmaprs727504814
1000 genomesrs727504814
hgdprs727504814
ensemblrs727504814
gopubmedrs727504814
geneviewrs727504814
scholarrs727504814
googlers727504814
pharmgkbrs727504814
gwascentralrs727504814
openSNPrs727504814
23andMers727504814
23andMe allrs727504814
SNP Nexus

SNPshotrs727504814
SNPdbers727504814
MSV3drs727504814
GWAS Ctlgrs727504814
Max Magnitude0
ClinVar
Risk rs727504814(G;G)
Alt rs727504814(G;G)
Reference rs727504814(T;T)
Significance Pathogenic
Disease Hypohidrotic X-linked ectodermal dysplasia Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic X-linked ectodermal dysplasia Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.68836550T>C; NC_000023.10:g.68836550T>G
CLNSRC
CLNACC RCV000173251.1, RCV000156149.1,