rs777022647

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs777022647(C;T)

Make rs777022647(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

2

Position

108929342

Gene	EDAR, RANBP2

is a	snp
is	mentioned by
dbSNP	rs777022647
dbSNP (classic)	rs777022647
ClinGen	rs777022647
ebi	rs777022647
HLI	rs777022647
Exac	rs777022647
Gnomad	rs777022647
Varsome	rs777022647
LitVar	rs777022647
Map	rs777022647
PheGenI	rs777022647
Biobank	rs777022647
1000 genomes	rs777022647
hgdp	rs777022647
ensembl	rs777022647
geneview	rs777022647
scholar	rs777022647
google	rs777022647
pharmgkb	rs777022647
gwascentral	rs777022647
openSNP	rs777022647
23andMe	rs777022647
SNPshot	rs777022647
SNPdbe	rs777022647
MSV3d	rs777022647
GWAS Ctlg	rs777022647

Max Magnitude

0

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,