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rs786201032

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786201032(C;T)
Make rs786201032(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position299372
GeneIFITM5
is asnp
is mentioned by
dbSNPrs786201032
ebirs786201032
HLIrs786201032
Exacrs786201032
Varsomers786201032
Maprs786201032
PheGenIrs786201032
hapmaprs786201032
1000 genomesrs786201032
hgdprs786201032
ensemblrs786201032
gopubmedrs786201032
geneviewrs786201032
scholarrs786201032
googlers786201032
pharmgkbrs786201032
gwascentralrs786201032
openSNPrs786201032
23andMers786201032
23andMe allrs786201032
SNP Nexus

SNPshotrs786201032
SNPdbers786201032
MSV3drs786201032
GWAS Ctlgrs786201032
Max Magnitude0
ClinVar
Risk rs786201032(T;T)
Alt rs786201032(T;T)
Reference rs786201032(C;C)
Significance Pathogenic
Disease Osteogenesis imperfecta type 5
Variation info
Gene IFITM5
CLNDBN Osteogenesis imperfecta type 5
Reversed 1
HGVS NC_000011.9:g.299372G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000162330.3,