rs1800561

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs1800561(C;T)

Make rs1800561(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

15824935

Gene

CD38

is a	snp
is	mentioned by
dbSNP	rs1800561
dbSNP (classic)	rs1800561
ClinGen	rs1800561
ebi	rs1800561
HLI	rs1800561
Exac	rs1800561
Gnomad	rs1800561
Varsome	rs1800561
LitVar	rs1800561
Map	rs1800561
PheGenI	rs1800561
Biobank	rs1800561
1000 genomes	rs1800561
hgdp	rs1800561
ensembl	rs1800561
geneview	rs1800561
scholar	rs1800561
google	rs1800561
pharmgkb	rs1800561
gwascentral	rs1800561
openSNP	rs1800561
23andMe	rs1800561
SNPshot	rs1800561
SNPdbe	rs1800561
MSV3d	rs1800561
GWAS Ctlg	rs1800561

GMAF

0.001837

Max Magnitude

0

[PMID 19240243] CD38 gene polymorphisms contribute to genetic susceptibility to B-cell chronic lymphocytic leukemia: evidence from two case-control studies in polish Caucasians.

[PMID 22366648] Social memory, amnesia, and autism: Brain oxytocin secretion is regulated by NAD(+) metabolites and single nucleotide polymorphisms of CD38

[PMID 20435366] Two genetic variants of CD38 in subjects with autism spectrum disorder and controls.

[PMID 24313001] [CD38 and autism spectrum disorders]

[PMID 26025338] The CD38 genotype (rs1800561 (4693C>T): R140W) is associated with an increased risk of admission to the neonatal intensive care unit