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rs786205627

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205627(-;-)
Make rs786205627(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position30987004
GeneHSD3B7
is asnp
is mentioned by
dbSNPrs786205627
ebirs786205627
HLIrs786205627
Exacrs786205627
Varsomers786205627
Maprs786205627
PheGenIrs786205627
hapmaprs786205627
1000 genomesrs786205627
hgdprs786205627
ensemblrs786205627
gopubmedrs786205627
geneviewrs786205627
scholarrs786205627
googlers786205627
pharmgkbrs786205627
gwascentralrs786205627
openSNPrs786205627
23andMers786205627
23andMe allrs786205627
SNP Nexus

SNPshotrs786205627
SNPdbers786205627
MSV3drs786205627
GWAS Ctlgrs786205627
Max Magnitude0
ClinVar
Risk rs786205627(;)
Alt rs786205627(;)
Reference rs786205627(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HSD3B7
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.30998325delT
CLNSRC
CLNACC RCV000171481.1,