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rs777425801

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs777425801(C;T)
Make rs777425801(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position71441413
GeneDHCR7
is asnp
is mentioned by
dbSNPrs777425801
dbSNP (classic)rs777425801
ClinGenrs777425801
ebirs777425801
HLIrs777425801
Exacrs777425801
Gnomadrs777425801
Varsomers777425801
LitVarrs777425801
Maprs777425801
PheGenIrs777425801
Biobankrs777425801
1000 genomesrs777425801
hgdprs777425801
ensemblrs777425801
geneviewrs777425801
scholarrs777425801
googlers777425801
pharmgkbrs777425801
gwascentralrs777425801
openSNPrs777425801
23andMers777425801
SNPshotrs777425801
SNPdbers777425801
MSV3drs777425801
GWAS Ctlgrs777425801
Max Magnitude0
ClinVar
Risk rs777425801(T;T)
Alt rs777425801(T;T)
Reference Rs777425801(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DHCR7
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.71152459C>T
CLNSRC
CLNACC RCV000421810.1,