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rs886039348

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039348(A;A)
Make rs886039348(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position108897133
GeneEDAR, RANBP2
is asnp
is mentioned by
dbSNPrs886039348
dbSNP (old)rs886039348
ClinGenrs886039348
ebirs886039348
HLIrs886039348
Exacrs886039348
Gnomadrs886039348
Varsomers886039348
Maprs886039348
PheGenIrs886039348
Biobankrs886039348
1000 genomesrs886039348
hgdprs886039348
ensemblrs886039348
gopubmedrs886039348
geneviewrs886039348
scholarrs886039348
googlers886039348
pharmgkbrs886039348
gwascentralrs886039348
openSNPrs886039348
23andMers886039348
23andMe allrs886039348
SNP Nexus

SNPshotrs886039348
SNPdbers886039348
MSV3drs886039348
GWAS Ctlgrs886039348
Max Magnitude0
ClinVar
Risk rs886039348(A;A) rs886039348(T;T)
Alt rs886039348(A;A) rs886039348(T;T)
Reference Rs886039348(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene EDAR
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.109513589C>T
CLNSRC
CLNACC RCV000256050.1,