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rs786205642

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205642(A;A)
Make rs786205642(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome21
Position46125812
GeneCOL6A2
is asnp
is mentioned by
dbSNPrs786205642
ebirs786205642
HLIrs786205642
Exacrs786205642
Varsomers786205642
Maprs786205642
PheGenIrs786205642
hapmaprs786205642
1000 genomesrs786205642
hgdprs786205642
ensemblrs786205642
gopubmedrs786205642
geneviewrs786205642
scholarrs786205642
googlers786205642
pharmgkbrs786205642
gwascentralrs786205642
openSNPrs786205642
23andMers786205642
23andMe allrs786205642
SNP Nexus

SNPshotrs786205642
SNPdbers786205642
MSV3drs786205642
GWAS Ctlgrs786205642
Max Magnitude0
ClinVar
Risk rs786205642(A;A)
Alt rs786205642(A;A)
Reference rs786205642(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL6A2
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.47545726G>A
CLNSRC
CLNACC RCV000171510.1,