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rs61767072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGGGCGGGGCCG;GGGGCGGGGCCG) 0 common in clinvar
(GGGGGCGGGGCC;GGGGGCGGGGCC) 0 common in clinvar
Make rs61767072(-;-)
Make rs61767072(-;GGGGCGGGGCCG)
ReferenceGRCh38 38.1/142
Chromosome4
Position3767570
GeneADRA2C, LOC107986251
is asnp
is mentioned by
dbSNPrs61767072
dbSNP (classic)rs61767072
ClinGenrs61767072
ebirs61767072
HLIrs61767072
Exacrs61767072
Gnomadrs61767072
Varsomers61767072
LitVarrs61767072
Maprs61767072
PheGenIrs61767072
Biobankrs61767072
1000 genomesrs61767072
hgdprs61767072
ensemblrs61767072
geneviewrs61767072
scholarrs61767072
googlers61767072
pharmgkbrs61767072
gwascentralrs61767072
openSNPrs61767072
23andMers61767072
SNPshotrs61767072
SNPdbers61767072
MSV3drs61767072
GWAS Ctlgrs61767072
Max Magnitude0
ClinVar
Risk rs61767072(-;-) Rs61767072(GGGGGCGGGGCC;GGGGGCGGGGCC)
Alt rs61767072(-;-) Rs61767072(GGGGGCGGGGCC;GGGGGCGGGGCC)
Reference Rs61767072(GGGGCGGGGCCG;GGGGCGGGGCCG)
Significance Drug-response
Disease Congestive heart failure and beta-blocker response
Variation info
Gene ADRA2C
CLNDBN Congestive heart failure and beta-blocker response, modifier of
Reversed 0
HGVS NC_000004.11:g.3769297_3769308delGGGGCGGGGCCG
CLNSRC OMIM Allelic Variant
CLNACC RCV000019790.2,