rs2229857

minus

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

Make rs2229857(A;G)

Make rs2229857(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

154601491

Gene

ADAR

is a	snp
is	mentioned by
dbSNP	rs2229857
dbSNP (classic)	rs2229857
ClinGen	rs2229857
ebi	rs2229857
HLI	rs2229857
Exac	rs2229857
Gnomad	rs2229857
Varsome	rs2229857
LitVar	rs2229857
Map	rs2229857
PheGenI	rs2229857
Biobank	rs2229857
1000 genomes	rs2229857
hgdp	rs2229857
ensembl	rs2229857
geneview	rs2229857
scholar	rs2229857
google	rs2229857
pharmgkb	rs2229857
gwascentral	rs2229857
openSNP	rs2229857
23andMe	rs2229857
SNPshot	rs2229857
SNPdbe	rs2229857
MSV3d	rs2229857
GWAS Ctlg	rs2229857

GMAF

0.3797

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

[PMID 21939710 ] Genetic polymorphisms in host antiviral genes: Associations with humoral and cellular immunity to measles vaccine

[PMID 19434718 ] Variants in interferon-alpha pathway genes and response to pegylated interferon-Alpha2a plus ribavirin for treatment of chronic hepatitis C virus infection in the hepatitis C antiviral long-term treatment against cirrhosis trial.

ClinVar
Risk	rs2229857(G;G)
Alt	rs2229857(G;G)
Reference	Rs2229857(A;A)
Significance	Non-pathogenic
Disease	not specified Symmetrical dyschromatosis of extremities
Variation	info
Gene	ADAR
CLNDBN	not specified Symmetrical dyschromatosis of extremities
Reversed	1
HGVS	NC_000001.10:g.154573967T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000175658.2, RCV000380536.1,