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rs794726670

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACT;ACT) 0 common in clinvar
Make rs794726670(-;-)
Make rs794726670(-;TAC)
Make rs794726670(TAC;TAC)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position67436680
GeneHSD11B2
is asnp
is mentioned by
dbSNPrs794726670
dbSNP (old)rs794726670
ClinGenrs794726670
ebirs794726670
HLIrs794726670
Exacrs794726670
Varsomers794726670
Maprs794726670
PheGenIrs794726670
Biobankrs794726670
1000 genomesrs794726670
hgdprs794726670
ensemblrs794726670
gopubmedrs794726670
geneviewrs794726670
scholarrs794726670
googlers794726670
pharmgkbrs794726670
gwascentralrs794726670
openSNPrs794726670
23andMers794726670
23andMe allrs794726670
SNP Nexus

SNPshotrs794726670
SNPdbers794726670
MSV3drs794726670
GWAS Ctlgrs794726670
Max Magnitude0
ClinVar
Risk rs794726670(-;-)
Alt rs794726670(-;-)
Reference Rs794726670(ACT;ACT)
Significance Pathogenic
Disease Apparent mineralocorticoid excess
Variation info
Gene HSD11B2
CLNDBN Apparent mineralocorticoid excess
Reversed 0
HGVS NC_000016.9:g.67470583_67470585delTAC
CLNSRC OMIM Allelic Variant
CLNACC RCV000012884.4,