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rs786205578

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205578(A;A)
Make rs786205578(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position33186771
GeneCOL11A2
is asnp
is mentioned by
dbSNPrs786205578
ebirs786205578
HLIrs786205578
Exacrs786205578
Varsomers786205578
Maprs786205578
PheGenIrs786205578
hapmaprs786205578
1000 genomesrs786205578
hgdprs786205578
ensemblrs786205578
gopubmedrs786205578
geneviewrs786205578
scholarrs786205578
googlers786205578
pharmgkbrs786205578
gwascentralrs786205578
openSNPrs786205578
23andMers786205578
23andMe allrs786205578
SNP Nexus

SNPshotrs786205578
SNPdbers786205578
MSV3drs786205578
GWAS Ctlgrs786205578
Max Magnitude0
ClinVar
Risk rs786205578(A;A)
Alt rs786205578(A;A)
Reference rs786205578(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL11A2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.33154548A>T
CLNSRC
CLNACC RCV000171393.1,