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rs464218

From SNPedia

Orientationminus
Make rs464218(C;C)
Make rs464218(C;T)
Make rs464218(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position109313684
GeneSORT1
is asnp
is mentioned by
dbSNPrs464218
ebirs464218
HLIrs464218
Exacrs464218
Varsomers464218
Maprs464218
PheGenIrs464218
hapmaprs464218
1000 genomesrs464218
hgdprs464218
ensemblrs464218
gopubmedrs464218
geneviewrs464218
scholarrs464218
googlers464218
pharmgkbrs464218
gwascentralrs464218
openSNPrs464218
23andMers464218
23andMe allrs464218
SNP Nexus

SNPshotrs464218
SNPdbers464218
MSV3drs464218
GWAS Ctlgrs464218
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 26464717OA-icon.png] Association of variants in CELSR2-PSRC1-SORT1 with risk of serum lipid traits, coronary artery disease and ischemic stroke