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rs1671021

From SNPedia

Orientationminus
Stabilizedminus
Make rs1671021(A;A)
Make rs1671021(A;G)
Make rs1671021(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position75569090
GeneLLGL2
is asnp
is mentioned by
dbSNPrs1671021
ebirs1671021
HLIrs1671021
Exacrs1671021
Varsomers1671021
Maprs1671021
PheGenIrs1671021
hapmaprs1671021
1000 genomesrs1671021
hgdprs1671021
ensemblrs1671021
gopubmedrs1671021
geneviewrs1671021
scholarrs1671021
googlers1671021
pharmgkbrs1671021
gwascentralrs1671021
openSNPrs1671021
23andMers1671021
23andMe allrs1671021
SNP Nexus

SNPshotrs1671021
SNPdbers1671021
MSV3drs1671021
GWAS Ctlgrs1671021
GMAF0.449
Max Magnitude
? (A;A) (A;G) (G;G) 28

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


GET Evidence
LLGL2-F479L
aa_change Phe479Leu
aa_change_short F479L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.537474
summary