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

rs80358231

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs80358231(A;A)
Make rs80358231(A;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position32298974
GeneMRAP
is asnp
is mentioned by
dbSNPrs80358231
ebirs80358231
HLIrs80358231
Exacrs80358231
Varsomers80358231
Maprs80358231
PheGenIrs80358231
hapmaprs80358231
1000 genomesrs80358231
hgdprs80358231
ensemblrs80358231
gopubmedrs80358231
geneviewrs80358231
scholarrs80358231
googlers80358231
pharmgkbrs80358231
gwascentralrs80358231
openSNPrs80358231
23andMers80358231
23andMe allrs80358231
SNP Nexus

SNPshotrs80358231
SNPdbers80358231
MSV3drs80358231
GWAS Ctlgrs80358231
Max Magnitude0
OMIM609196
Desc
Variant0006
Relatedalso
ClinVar
Risk rs80358231(A;A)
Alt rs80358231(A;A)
Reference rs80358231(G;G)
Significance Pathogenic
Disease Glucocorticoid deficiency 2
Variation info
Gene MRAP
CLNDBN Glucocorticoid deficiency 2
Reversed 0
HGVS NC_000021.8:g.33671285G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001915.2,