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rs387907009

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907009(G;T)
Make rs387907009(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position121790166
GeneIQCB1
is asnp
is mentioned by
dbSNPrs387907009
ebirs387907009
HLIrs387907009
Exacrs387907009
Varsomers387907009
Maprs387907009
PheGenIrs387907009
hapmaprs387907009
1000 genomesrs387907009
hgdprs387907009
ensemblrs387907009
gopubmedrs387907009
geneviewrs387907009
scholarrs387907009
googlers387907009
pharmgkbrs387907009
gwascentralrs387907009
openSNPrs387907009
23andMers387907009
23andMe allrs387907009
SNP Nexus

SNPshotrs387907009
SNPdbers387907009
MSV3drs387907009
GWAS Ctlgrs387907009
Max Magnitude0
ClinVar
Risk rs387907009(T;T)
Alt rs387907009(T;T)
Reference rs387907009(G;G)
Significance Pathogenic
Disease Senior-Loken syndrome 5
Variation info
Gene IQCB1
CLNDBN Senior-Loken syndrome 5
Reversed 1
HGVS NC_000003.11:g.121509013C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023758.4,