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rs149733264

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs149733264(C;C)
Make rs149733264(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position36754358
GeneHLCS
is asnp
is mentioned by
dbSNPrs149733264
ebirs149733264
HLIrs149733264
Exacrs149733264
Varsomers149733264
Maprs149733264
PheGenIrs149733264
hapmaprs149733264
1000 genomesrs149733264
hgdprs149733264
ensemblrs149733264
gopubmedrs149733264
geneviewrs149733264
scholarrs149733264
googlers149733264
pharmgkbrs149733264
gwascentralrs149733264
openSNPrs149733264
23andMers149733264
23andMe allrs149733264
SNP Nexus

SNPshotrs149733264
SNPdbers149733264
MSV3drs149733264
GWAS Ctlgrs149733264
Max Magnitude0
ClinVar
Risk rs149733264(C;C)
Alt rs149733264(C;C)
Reference rs149733264(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HLCS
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.38126659T>A
CLNSRC
CLNACC RCV000185964.1,