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rs876657684

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876657684(-;-)
Make rs876657684(-;GGGC)
Make rs876657684(GGGC;GGGC)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position69616630
GeneEDA
is asnp
is mentioned by
dbSNPrs876657684
ebirs876657684
HLIrs876657684
Exacrs876657684
Varsomers876657684
Maprs876657684
PheGenIrs876657684
hapmaprs876657684
1000 genomesrs876657684
hgdprs876657684
ensemblrs876657684
gopubmedrs876657684
geneviewrs876657684
scholarrs876657684
googlers876657684
pharmgkbrs876657684
gwascentralrs876657684
openSNPrs876657684
23andMers876657684
23andMe allrs876657684
SNP Nexus

SNPshotrs876657684
SNPdbers876657684
MSV3drs876657684
GWAS Ctlgrs876657684
Max Magnitude0
ClinVar
Risk rs876657684(GGGC;GGGC)
Alt rs876657684(GGGC;GGGC)
Reference rs876657684(;)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.68836471_68836474dupGGGC
CLNSRC
CLNACC RCV000213343.1,