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rs397516660

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516660(A;A)
Make rs397516660(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position69616637
GeneEDA
is asnp
is mentioned by
dbSNPrs397516660
ebirs397516660
HLIrs397516660
Exacrs397516660
Varsomers397516660
Maprs397516660
PheGenIrs397516660
hapmaprs397516660
1000 genomesrs397516660
hgdprs397516660
ensemblrs397516660
gopubmedrs397516660
geneviewrs397516660
scholarrs397516660
googlers397516660
pharmgkbrs397516660
gwascentralrs397516660
openSNPrs397516660
23andMers397516660
23andMe allrs397516660
SNP Nexus

SNPshotrs397516660
SNPdbers397516660
MSV3drs397516660
GWAS Ctlgrs397516660
Max Magnitude0
ClinVar
Risk rs397516660(A;A)
Alt rs397516660(A;A)
Reference rs397516660(C;C)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.68836481C>A
CLNSRC ClinVar
CLNACC RCV000037167.2,