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rs727505089

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs727505089(-;-)
Make rs727505089(-;GGGT)
Make rs727505089(GGGT;GGGT)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position69616443
GeneEDA
is asnp
is mentioned by
dbSNPrs727505089
ebirs727505089
HLIrs727505089
Exacrs727505089
Varsomers727505089
Maprs727505089
PheGenIrs727505089
hapmaprs727505089
1000 genomesrs727505089
hgdprs727505089
ensemblrs727505089
gopubmedrs727505089
geneviewrs727505089
scholarrs727505089
googlers727505089
pharmgkbrs727505089
gwascentralrs727505089
openSNPrs727505089
23andMers727505089
23andMe allrs727505089
SNP Nexus

SNPshotrs727505089
SNPdbers727505089
MSV3drs727505089
GWAS Ctlgrs727505089
Max Magnitude0
ClinVar
Risk rs727505089(TGGG;TGGG)
Alt rs727505089(TGGG;TGGG)
Reference rs727505089(;)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.68836284_68836287dupGGGT
CLNSRC
CLNACC RCV000156531.1,