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rs1800561

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1800561(C;T)
Make rs1800561(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position15824935
GeneCD38
is asnp
is mentioned by
dbSNPrs1800561
ebirs1800561
HLIrs1800561
Exacrs1800561
Varsomers1800561
Maprs1800561
PheGenIrs1800561
hapmaprs1800561
1000 genomesrs1800561
hgdprs1800561
ensemblrs1800561
gopubmedrs1800561
geneviewrs1800561
scholarrs1800561
googlers1800561
pharmgkbrs1800561
gwascentralrs1800561
openSNPrs1800561
23andMers1800561
23andMe allrs1800561
SNP Nexus

SNPshotrs1800561
SNPdbers1800561
MSV3drs1800561
GWAS Ctlgrs1800561
GMAF0.001837
Max Magnitude0

[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