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

rs281864801

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0 common genotype
(TTATTT;TTATTT) 0 common in clinvar
(TTTTTA;TTTTTA) 0 common in clinvar
Make rs281864801(-;-)
Make rs281864801(-;TTTTTA)
ReferenceGRCh38 38.1/141
Chromosome17
Position68527833
GenePRKAR1A
is asnp
is mentioned by
dbSNPrs281864801
dbSNP (classic)rs281864801
ClinGenrs281864801
ebirs281864801
HLIrs281864801
Exacrs281864801
Gnomadrs281864801
Varsomers281864801
LitVarrs281864801
Maprs281864801
PheGenIrs281864801
Biobankrs281864801
1000 genomesrs281864801
hgdprs281864801
ensemblrs281864801
geneviewrs281864801
scholarrs281864801
googlers281864801
pharmgkbrs281864801
gwascentralrs281864801
openSNPrs281864801
23andMers281864801
SNPshotrs281864801
SNPdbers281864801
MSV3drs281864801
GWAS Ctlgrs281864801
Max Magnitude0
ClinVar
Risk rs281864801(-;-)
Alt rs281864801(-;-)
Reference Rs281864801(TTATTT;TTATTT)
Significance Pathogenic
Disease Pigmented nodular adrenocortical disease Carney complex
Variation info
Gene PRKAR1A
CLNDBN Pigmented nodular adrenocortical disease, primary, 1 Carney complex
Reversed 0
HGVS NC_000017.10:g.66523974_66523979delTTTTTA
CLNSRC OMIM Allelic Variant
CLNACC RCV000013511.24, RCV000013512.25,