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rs776969714

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(D;D) 0 common genotype
Make rs776969714(-;C)
Make rs776969714(C;C)
ReferenceGRCh38.p7 38.3/149
Chromosome4
Position25145129
GeneSEPSECS
is asnp
is mentioned by
dbSNPrs776969714
dbSNP (classic)rs776969714
ClinGenrs776969714
ebirs776969714
HLIrs776969714
Exacrs776969714
Gnomadrs776969714
Varsomers776969714
LitVarrs776969714
Maprs776969714
PheGenIrs776969714
Biobankrs776969714
1000 genomesrs776969714
hgdprs776969714
ensemblrs776969714
geneviewrs776969714
scholarrs776969714
googlers776969714
pharmgkbrs776969714
gwascentralrs776969714
openSNPrs776969714
23andMers776969714
23andMe allrs776969714
SNPshotrs776969714
SNPdbers776969714
MSV3drs776969714
GWAS Ctlgrs776969714
Max Magnitude0
ClinVar
Risk rs776969714(C;C)
Alt rs776969714(C;C)
Reference Rs776969714(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene SEPSECS
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.25146752dupC
CLNSRC
CLNACC RCV000396553.1,