rs1057520217

Orientation

minus

Stabilized

minus

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

Make rs1057520217(C;T)

Make rs1057520217(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

44651601

Gene

ADA

is a	snp
is	mentioned by
dbSNP	rs1057520217
dbSNP (classic)	rs1057520217
ClinGen	rs1057520217
ebi	rs1057520217
HLI	rs1057520217
Exac	rs1057520217
Gnomad	rs1057520217
Varsome	rs1057520217
LitVar	rs1057520217
Map	rs1057520217
PheGenI	rs1057520217
Biobank	rs1057520217
1000 genomes	rs1057520217
hgdp	rs1057520217
ensembl	rs1057520217
geneview	rs1057520217
scholar	rs1057520217
google	rs1057520217
pharmgkb	rs1057520217
gwascentral	rs1057520217
openSNP	rs1057520217
23andMe	rs1057520217
SNPshot	rs1057520217
SNPdbe	rs1057520217
MSV3d	rs1057520217
GWAS Ctlg	rs1057520217

Max Magnitude

0

ClinVar
Risk	rs1057520217(T;T)
Alt	rs1057520217(T;T)
Reference	Rs1057520217(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ADA
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.43280242G>A
CLNSRC
CLNACC	RCV000433743.1,