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rs1064793684

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAGGGCT;CAGGGCT) 0 common in clinvar
Chromosome2
Position108907934
GeneEDAR, RANBP2
is asnp
is mentioned by
dbSNPrs1064793684
dbSNP (classic)rs1064793684
ClinGenrs1064793684
ebirs1064793684
HLIrs1064793684
Exacrs1064793684
Gnomadrs1064793684
Varsomers1064793684
LitVarrs1064793684
Maprs1064793684
PheGenIrs1064793684
Biobankrs1064793684
1000 genomesrs1064793684
hgdprs1064793684
ensemblrs1064793684
geneviewrs1064793684
scholarrs1064793684
googlers1064793684
pharmgkbrs1064793684
gwascentralrs1064793684
openSNPrs1064793684
23andMers1064793684
SNPshotrs1064793684
SNPdbers1064793684
MSV3drs1064793684
GWAS Ctlgrs1064793684
Max Magnitude0
ClinVar
Risk rs1064793684(TGATGAGGAGCCCG;TGATGAGGAGCCCG)
Alt rs1064793684(TGATGAGGAGCCCG;TGATGAGGAGCCCG)
Reference Rs1064793684(CAGGGCT;CAGGGCT)
Significance Pathogenic
Disease not provided
Variation info
Gene EDAR
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.109524390_109524396delAGCCCTGinsCGGGCTCCTCATCA
CLNSRC
CLNACC RCV000485277.1,