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rs786205587

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205587(A;A)
Make rs786205587(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position94410465
GeneCOL1A2
is asnp
is mentioned by
dbSNPrs786205587
ebirs786205587
HLIrs786205587
Exacrs786205587
Varsomers786205587
Maprs786205587
PheGenIrs786205587
hapmaprs786205587
1000 genomesrs786205587
hgdprs786205587
ensemblrs786205587
gopubmedrs786205587
geneviewrs786205587
scholarrs786205587
googlers786205587
pharmgkbrs786205587
gwascentralrs786205587
openSNPrs786205587
23andMers786205587
23andMe allrs786205587
SNP Nexus

SNPshotrs786205587
SNPdbers786205587
MSV3drs786205587
GWAS Ctlgrs786205587
Max Magnitude0
ClinVar
Risk rs786205587(A;A)
Alt rs786205587(A;A)
Reference rs786205587(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL1A2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.94039777G>A
CLNSRC
CLNACC RCV000171409.1,