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rs6555546

From SNPedia

Orientationplus
Stabilizedplus
Make rs6555546(A;A)
Make rs6555546(A;C)
Make rs6555546(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position8440791
GeneSNORD19B
is asnp
is mentioned by
dbSNPrs6555546
ebirs6555546
HLIrs6555546
Exacrs6555546
Varsomers6555546
Maprs6555546
PheGenIrs6555546
hapmaprs6555546
1000 genomesrs6555546
hgdprs6555546
ensemblrs6555546
gopubmedrs6555546
geneviewrs6555546
scholarrs6555546
googlers6555546
pharmgkbrs6555546
gwascentralrs6555546
openSNPrs6555546
23andMers6555546
23andMe allrs6555546
SNP Nexus

SNPshotrs6555546
SNPdbers6555546
MSV3drs6555546
GWAS Ctlgrs6555546
GMAF0.2658
Max Magnitude
? (A;A) (A;C) (C;C) 28


GET Evidence
rs6555546
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.3125
summary