rs761242509

Orientation

plus

Stabilized

plus

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

Make rs761242509(C;T)

Make rs761242509(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

20

Position

44625568

Gene

ADA

is a	snp
is	mentioned by
dbSNP	rs761242509
dbSNP (classic)	rs761242509
ClinGen	rs761242509
ebi	rs761242509
HLI	rs761242509
Exac	rs761242509
Gnomad	rs761242509
Varsome	rs761242509
LitVar	rs761242509
Map	rs761242509
PheGenI	rs761242509
Biobank	rs761242509
1000 genomes	rs761242509
hgdp	rs761242509
ensembl	rs761242509
geneview	rs761242509
scholar	rs761242509
google	rs761242509
pharmgkb	rs761242509
gwascentral	rs761242509
openSNP	rs761242509
23andMe	rs761242509
SNPshot	rs761242509
SNPdbe	rs761242509
MSV3d	rs761242509
GWAS Ctlg	rs761242509

Max Magnitude

0

ClinVar
Risk	rs761242509(T;T)
Alt	rs761242509(T;T)
Reference	Rs761242509(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ADA
CLNDBN	not provided
Reversed	0
HGVS	NC_000020.10:g.43254209C>T
CLNSRC
CLNACC	RCV000254941.1,