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rs2518824

From SNPedia

Orientationplus
Stabilizedplus
Make rs2518824(G;G)
Make rs2518824(G;T)
Make rs2518824(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19975440
GeneARVCF
is asnp
is mentioned by
dbSNPrs2518824
ebirs2518824
HLIrs2518824
Exacrs2518824
Varsomers2518824
Maprs2518824
PheGenIrs2518824
hapmaprs2518824
1000 genomesrs2518824
hgdprs2518824
ensemblrs2518824
gopubmedrs2518824
geneviewrs2518824
scholarrs2518824
googlers2518824
pharmgkbrs2518824
gwascentralrs2518824
openSNPrs2518824
23andMers2518824
23andMe allrs2518824
SNP Nexus

SNPshotrs2518824
SNPdbers2518824
MSV3drs2518824
GWAS Ctlgrs2518824
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 24819575] Common genetic variants and risk of brain injury after preterm birth