Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205678

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205678(C;T)
Make rs786205678(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position40354320
GeneRARA
is asnp
is mentioned by
dbSNPrs786205678
ebirs786205678
HLIrs786205678
Exacrs786205678
Varsomers786205678
Maprs786205678
PheGenIrs786205678
hapmaprs786205678
1000 genomesrs786205678
hgdprs786205678
ensemblrs786205678
gopubmedrs786205678
geneviewrs786205678
scholarrs786205678
googlers786205678
pharmgkbrs786205678
gwascentralrs786205678
openSNPrs786205678
23andMers786205678
23andMe allrs786205678
SNP Nexus

SNPshotrs786205678
SNPdbers786205678
MSV3drs786205678
GWAS Ctlgrs786205678
Max Magnitude0
ClinVar
Risk rs786205678(T;T)
Alt rs786205678(T;T)
Reference rs786205678(C;C)
Significance Drug-response
Disease all trans retinoic acid (ATRA) response
Variation info
Gene RARA
CLNDBN all trans retinoic acid (ATRA) response
Reversed 0
HGVS NC_000017.10:g.38510572C>T
CLNSRC
CLNACC RCV000171542.1,