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rs757504141

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs757504141(C;C)
Make rs757504141(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position25156853
GeneSEPSECS
is asnp
is mentioned by
dbSNPrs757504141
dbSNP (classic)rs757504141
ClinGenrs757504141
ebirs757504141
HLIrs757504141
Exacrs757504141
Gnomadrs757504141
Varsomers757504141
LitVarrs757504141
Maprs757504141
PheGenIrs757504141
Biobankrs757504141
1000 genomesrs757504141
hgdprs757504141
ensemblrs757504141
geneviewrs757504141
scholarrs757504141
googlers757504141
pharmgkbrs757504141
gwascentralrs757504141
openSNPrs757504141
23andMers757504141
23andMe allrs757504141
SNPshotrs757504141
SNPdbers757504141
MSV3drs757504141
GWAS Ctlgrs757504141
Max Magnitude0
ClinVar
Risk rs757504141(C;C)
Alt rs757504141(C;C)
Reference Rs757504141(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SEPSECS
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.25158475T>C
CLNSRC
CLNACC RCV000428576.1,