rs771266745

Orientation

plus

Stabilized

plus

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

Make rs771266745(-;-)

Make rs771266745(-;TTCTC)

Make rs771266745(TTCTC;TTCTC)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

44621033

Gene

ADA

is a	snp
is	mentioned by
dbSNP	rs771266745
dbSNP (classic)	rs771266745
ClinGen	rs771266745
ebi	rs771266745
HLI	rs771266745
Exac	rs771266745
Gnomad	rs771266745
Varsome	rs771266745
LitVar	rs771266745
Map	rs771266745
PheGenI	rs771266745
Biobank	rs771266745
1000 genomes	rs771266745
hgdp	rs771266745
ensembl	rs771266745
geneview	rs771266745
scholar	rs771266745
google	rs771266745
pharmgkb	rs771266745
gwascentral	rs771266745
openSNP	rs771266745
23andMe	rs771266745
SNPshot	rs771266745
SNPdbe	rs771266745
MSV3d	rs771266745
GWAS Ctlg	rs771266745

Max Magnitude

0

ClinVar
Risk	rs771266745(-;-)
Alt	rs771266745(-;-)
Reference	Rs771266745(CTCTT;CTCTT)
Significance	Other
Disease	Severe combined immunodeficiency due to ADA deficiency not provided
Variation	info
Gene	ADA
CLNDBN	Severe combined immunodeficiency due to ADA deficiency not provided
Reversed	0
HGVS	NC_000020.10:g.43249674_43249678delCTCTT
CLNSRC
CLNACC	RCV000173618.1, RCV000255208.1,