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rs121917877

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917877(C;T)
Make rs121917877(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position1079586
GeneSSTR5
is asnp
is mentioned by
dbSNPrs121917877
ebirs121917877
HLIrs121917877
Exacrs121917877
Varsomers121917877
Maprs121917877
PheGenIrs121917877
hapmaprs121917877
1000 genomesrs121917877
hgdprs121917877
ensemblrs121917877
gopubmedrs121917877
geneviewrs121917877
scholarrs121917877
googlers121917877
pharmgkbrs121917877
gwascentralrs121917877
openSNPrs121917877
23andMers121917877
23andMe allrs121917877
SNP Nexus

SNPshotrs121917877
SNPdbers121917877
MSV3drs121917877
GWAS Ctlgrs121917877
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs121917877(T;T)
Alt rs121917877(T;T)
Reference rs121917877(C;C)
Significance Other
Disease Somatostatin analog
Variation info
Gene SSTR5 SSTR5-AS1
CLNDBN Somatostatin analog, resistance to
Reversed 0
HGVS NC_000016.9:g.1129586C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013734.18,