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rs794726669

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTGGAG;TTGGAG) 0 common in clinvar
Make rs794726669(-;-)
Make rs794726669(-;GAGTTG)
Make rs794726669(GAGTTG;GAGTTG)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position67435705
GeneHSD11B2
is asnp
is mentioned by
dbSNPrs794726669
dbSNP (old)rs794726669
ClinGenrs794726669
ebirs794726669
HLIrs794726669
Exacrs794726669
Gnomadrs794726669
Varsomers794726669
Maprs794726669
PheGenIrs794726669
Biobankrs794726669
1000 genomesrs794726669
hgdprs794726669
ensemblrs794726669
gopubmedrs794726669
geneviewrs794726669
scholarrs794726669
googlers794726669
pharmgkbrs794726669
gwascentralrs794726669
openSNPrs794726669
23andMers794726669
23andMe allrs794726669
SNP Nexus

SNPshotrs794726669
SNPdbers794726669
MSV3drs794726669
GWAS Ctlgrs794726669
Max Magnitude0
ClinVar
Risk rs794726669(-;-)
Alt rs794726669(-;-)
Reference Rs794726669(TTGGAG;TTGGAG)
Significance Pathogenic
Disease Apparent mineralocorticoid excess
Variation info
Gene HSD11B2
CLNDBN Apparent mineralocorticoid excess, mild
Reversed 0
HGVS NC_000016.9:g.67469608_67469613delGAGTTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000012882.5,