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rs1062708

From SNPedia

Orientationplus
Stabilizedplus
Make rs1062708(C;C)
Make rs1062708(C;T)
Make rs1062708(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position49010016
GeneMIR6798, RUVBL2
is asnp
is mentioned by
dbSNPrs1062708
ebirs1062708
HLIrs1062708
Exacrs1062708
Varsomers1062708
Maprs1062708
PheGenIrs1062708
hapmaprs1062708
1000 genomesrs1062708
hgdprs1062708
ensemblrs1062708
gopubmedrs1062708
geneviewrs1062708
scholarrs1062708
googlers1062708
pharmgkbrs1062708
gwascentralrs1062708
openSNPrs1062708
23andMers1062708
23andMe allrs1062708
SNP Nexus

SNPshotrs1062708
SNPdbers1062708
MSV3drs1062708
GWAS Ctlgrs1062708
GMAF0.427
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19403135] Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study

[PMID 16251468OA-icon.png] Survey of allelic expression using EST mining.

[PMID 19052777OA-icon.png] Identification of common genetic variants that account for transcript isoform variation between human populations.

[PMID 19374514OA-icon.png] Expression and alternative splicing of folate pathway genes in HapMap lymphoblastoid cell lines.