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

rs876657642

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657642(A;C)
Make rs876657642(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position70033515
GeneEDA
is asnp
is mentioned by
dbSNPrs876657642
ebirs876657642
HLIrs876657642
Exacrs876657642
Varsomers876657642
Maprs876657642
PheGenIrs876657642
hapmaprs876657642
1000 genomesrs876657642
hgdprs876657642
ensemblrs876657642
gopubmedrs876657642
geneviewrs876657642
scholarrs876657642
googlers876657642
pharmgkbrs876657642
gwascentralrs876657642
openSNPrs876657642
23andMers876657642
23andMe allrs876657642
SNP Nexus

SNPshotrs876657642
SNPdbers876657642
MSV3drs876657642
GWAS Ctlgrs876657642
Max Magnitude0
ClinVar
Risk rs876657642(C;C)
Alt rs876657642(C;C)
Reference rs876657642(A;A)
Significance Probable-Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.69253365A>C
CLNSRC
CLNACC RCV000214953.1,