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rs2288904

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs2288904(C;C)
Make rs2288904(C;T)
Make rs2288904(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position10631494
GeneSLC44A2
is asnp
is mentioned by
dbSNPrs2288904
ebirs2288904
HLIrs2288904
Exacrs2288904
Varsomers2288904
Maprs2288904
PheGenIrs2288904
hapmaprs2288904
1000 genomesrs2288904
hgdprs2288904
ensemblrs2288904
gopubmedrs2288904
geneviewrs2288904
scholarrs2288904
googlers2288904
pharmgkbrs2288904
gwascentralrs2288904
openSNPrs2288904
23andMers2288904
23andMe allrs2288904
SNP Nexus

SNPshotrs2288904
SNPdbers2288904
MSV3drs2288904
GWAS Ctlgrs2288904
GMAF0.213
Max Magnitude0
? (C;C) (C;T) (T;T) 28

23andMe blog relevant for blood transfusion compatibility.

venous thromboembolism, [PMID 25772935OA-icon.png]

Venter snp
Source plos
Gene SLC44A2
allele G
frequency 0.767
sift TOLERATED
HuRef 1103691089575
Disease Association Possible antigen for autoimmune hearing loss.



OMIM606106
DescSOLUTE CARRIER FAMILY 44, MEMBER 2; SLC44A2
Variant
Relatedalso


GET Evidence
SLC44A2-Q154R
aa_change Gln154Arg
aa_change_short Q154R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.835843
summary



[PMID 24236643] HNA-3 gene frequencies in Brazilians and a new polymerase chain reaction-restriction fragment length polymorphism method for HNA-3a/3b genotyping


[PMID 25772935OA-icon.png] Meta-analysis of 65,734 Individuals Identifies TSPAN15 and SLC44A2 as Two Susceptibility Loci for Venous Thromboembolism


[PMID 26593331] Genotype frequency of human neutrophil antigen-3 polymorphisms in the Yi, Han, and Tibetan populations of China