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rs786205218

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205218(C;C)
Make rs786205218(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position22197420
GeneBMP1
is asnp
is mentioned by
dbSNPrs786205218
ebirs786205218
HLIrs786205218
Exacrs786205218
Varsomers786205218
Maprs786205218
PheGenIrs786205218
hapmaprs786205218
1000 genomesrs786205218
hgdprs786205218
ensemblrs786205218
gopubmedrs786205218
geneviewrs786205218
scholarrs786205218
googlers786205218
pharmgkbrs786205218
gwascentralrs786205218
openSNPrs786205218
23andMers786205218
23andMe allrs786205218
SNP Nexus

SNPshotrs786205218
SNPdbers786205218
MSV3drs786205218
GWAS Ctlgrs786205218
Max Magnitude0
ClinVar
Risk rs786205218(C;C)
Alt rs786205218(C;C)
Reference rs786205218(G;G)
Significance Pathogenic
Disease Osteogenesis imperfecta
Variation info
Gene BMP1
CLNDBN Osteogenesis imperfecta, type xiii
Reversed 0
HGVS NC_000008.10:g.22054933G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000170454.3,