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rs506770

From SNPedia

Orientationplus
Stabilizedplus
Make rs506770(C;C)
Make rs506770(C;G)
Make rs506770(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31817451
GeneHSPA1A, HSPA1L
is asnp
is mentioned by
dbSNPrs506770
ebirs506770
HLIrs506770
Exacrs506770
Varsomers506770
Maprs506770
PheGenIrs506770
hapmaprs506770
1000 genomesrs506770
hgdprs506770
ensemblrs506770
gopubmedrs506770
geneviewrs506770
scholarrs506770
googlers506770
pharmgkbrs506770
gwascentralrs506770
openSNPrs506770
23andMers506770
23andMe allrs506770
SNP Nexus

SNPshotrs506770
SNPdbers506770
MSV3drs506770
GWAS Ctlgrs506770
GMAF0.1657
Max Magnitude


GET Evidence
rs506770
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.841876
summary