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rs3130690

From SNPedia

Orientationminus
Stabilizedminus
Make rs3130690(A;A)
Make rs3130690(A;C)
Make rs3130690(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31318158
is asnp
is mentioned by
dbSNPrs3130690
ebirs3130690
HLIrs3130690
Exacrs3130690
Varsomers3130690
Maprs3130690
PheGenIrs3130690
hapmaprs3130690
1000 genomesrs3130690
hgdprs3130690
ensemblrs3130690
gopubmedrs3130690
geneviewrs3130690
scholarrs3130690
googlers3130690
pharmgkbrs3130690
gwascentralrs3130690
openSNPrs3130690
23andMers3130690
23andMe allrs3130690
SNP Nexus

SNPshotrs3130690
SNPdbers3130690
MSV3drs3130690
GWAS Ctlgrs3130690
GMAF0.1157
Max Magnitude
? (A;A) (A;C) (C;C) 28
OMIM608579
DescSEVERE CUTANEOUS ADVERSE REACTION, SUSCEPTIBILITY TO
Variant
Relatedalso





GET Evidence
rs3130690
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.131148
summary