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rs886039564

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039564(A;A)
Make rs886039564(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position108897181
GeneEDAR, RANBP2
is asnp
is mentioned by
dbSNPrs886039564
ClinGenrs886039564
ebirs886039564
HLIrs886039564
Exacrs886039564
Varsomers886039564
Maprs886039564
PheGenIrs886039564
Biobankrs886039564
1000 genomesrs886039564
hgdprs886039564
ensemblrs886039564
gopubmedrs886039564
geneviewrs886039564
scholarrs886039564
googlers886039564
pharmgkbrs886039564
gwascentralrs886039564
openSNPrs886039564
23andMers886039564
23andMe allrs886039564
SNP Nexus

SNPshotrs886039564
SNPdbers886039564
MSV3drs886039564
GWAS Ctlgrs886039564
Max Magnitude0
ClinVar
Risk rs886039564(A;A)
Alt rs886039564(A;A)
Reference Rs886039564(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene EDAR
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.109513637C>T
CLNSRC
CLNACC RCV000254918.1,