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rs786205506

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205506(A;A)
Make rs786205506(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position50190586
GeneCOL1A1
is asnp
is mentioned by
dbSNPrs786205506
ebirs786205506
HLIrs786205506
Exacrs786205506
Varsomers786205506
Maprs786205506
PheGenIrs786205506
hapmaprs786205506
1000 genomesrs786205506
hgdprs786205506
ensemblrs786205506
gopubmedrs786205506
geneviewrs786205506
scholarrs786205506
googlers786205506
pharmgkbrs786205506
gwascentralrs786205506
openSNPrs786205506
23andMers786205506
23andMe allrs786205506
SNP Nexus

SNPshotrs786205506
SNPdbers786205506
MSV3drs786205506
GWAS Ctlgrs786205506
Max Magnitude0
ClinVar
Risk rs786205506(A;A)
Alt rs786205506(A;A)
Reference rs786205506(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL1A1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.48267947C>T
CLNSRC
CLNACC RCV000171261.1,