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rs11853426

From SNPedia

Orientationplus
Stabilizedplus
Make rs11853426(C;C)
Make rs11853426(C;T)
Make rs11853426(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position60317231
is asnp
is mentioned by
dbSNPrs11853426
dbSNP (classic)rs11853426
ClinGenrs11853426
ebirs11853426
HLIrs11853426
Exacrs11853426
Gnomadrs11853426
Varsomers11853426
LitVarrs11853426
Maprs11853426
PheGenIrs11853426
Biobankrs11853426
1000 genomesrs11853426
hgdprs11853426
ensemblrs11853426
geneviewrs11853426
scholarrs11853426
googlers11853426
pharmgkbrs11853426
gwascentralrs11853426
openSNPrs11853426
23andMers11853426
SNPshotrs11853426
SNPdbers11853426
MSV3drs11853426
GWAS Ctlgrs11853426
GMAF0.4518
Max Magnitude0
? (C;C) (C;T) (T;T) 28


Part of a haplotype linked to stroke affecting perhaps 5% of sickle cell anemia patients