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rs786205505

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205505(G;G)
Make rs786205505(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position50189549
GeneCOL1A1
is asnp
is mentioned by
dbSNPrs786205505
ebirs786205505
HLIrs786205505
Exacrs786205505
Varsomers786205505
Maprs786205505
PheGenIrs786205505
hapmaprs786205505
1000 genomesrs786205505
hgdprs786205505
ensemblrs786205505
gopubmedrs786205505
geneviewrs786205505
scholarrs786205505
googlers786205505
pharmgkbrs786205505
gwascentralrs786205505
openSNPrs786205505
23andMers786205505
23andMe allrs786205505
SNP Nexus

SNPshotrs786205505
SNPdbers786205505
MSV3drs786205505
GWAS Ctlgrs786205505
Max Magnitude0
ClinVar
Risk rs786205505(G;G)
Alt rs786205505(G;G)
Reference rs786205505(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL1A1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.48266910A>C
CLNSRC
CLNACC RCV000171260.1,