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rs777022647

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs777022647(C;T)
Make rs777022647(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position108929342
GeneEDAR, RANBP2
is asnp
is mentioned by
dbSNPrs777022647
dbSNP (old)rs777022647
ClinGenrs777022647
ebirs777022647
HLIrs777022647
Exacrs777022647
Gnomadrs777022647
Varsomers777022647
Maprs777022647
PheGenIrs777022647
Biobankrs777022647
1000 genomesrs777022647
hgdprs777022647
ensemblrs777022647
gopubmedrs777022647
geneviewrs777022647
scholarrs777022647
googlers777022647
pharmgkbrs777022647
gwascentralrs777022647
openSNPrs777022647
23andMers777022647
23andMe allrs777022647
SNP Nexus

SNPshotrs777022647
SNPdbers777022647
MSV3drs777022647
GWAS Ctlgrs777022647
Max Magnitude0
ClinVar
Risk rs777022647(T;T)
Alt rs777022647(T;T)
Reference Rs777022647(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene EDAR
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.109545798C>T
CLNSRC
CLNACC RCV000256013.1,