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rs309844

From SNPedia

Orientationminus
Stabilizedplus
Make rs309844(C;C)
Make rs309844(C;T)
Make rs309844(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position29995847
is asnp
is mentioned by
dbSNPrs309844
ebirs309844
HLIrs309844
Exacrs309844
Varsomers309844
Maprs309844
PheGenIrs309844
hapmaprs309844
1000 genomesrs309844
hgdprs309844
ensemblrs309844
gopubmedrs309844
geneviewrs309844
scholarrs309844
googlers309844
pharmgkbrs309844
gwascentralrs309844
openSNPrs309844
23andMers309844
23andMe allrs309844
SNP Nexus

SNPshotrs309844
SNPdbers309844
MSV3drs309844
GWAS Ctlgrs309844
GMAF0.1511
Max Magnitude

[PMID 24322967] HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons Syndrome/Toxic Epidermal Necrolysis susceptibility in a population from Mozambique