Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205555

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205555(A;C)
Make rs786205555(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome21
Position45982664
GeneCOL6A1
is asnp
is mentioned by
dbSNPrs786205555
dbSNP (classic)rs786205555
ClinGenrs786205555
ebirs786205555
HLIrs786205555
Exacrs786205555
Gnomadrs786205555
Varsomers786205555
LitVarrs786205555
Maprs786205555
PheGenIrs786205555
Biobankrs786205555
1000 genomesrs786205555
hgdprs786205555
ensemblrs786205555
geneviewrs786205555
scholarrs786205555
googlers786205555
pharmgkbrs786205555
gwascentralrs786205555
openSNPrs786205555
23andMers786205555
SNPshotrs786205555
SNPdbers786205555
MSV3drs786205555
GWAS Ctlgrs786205555
Max Magnitude0
ClinVar
Risk rs786205555(C;C)
Alt rs786205555(C;C)
Reference Rs786205555(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL6A1
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.47402578A>C
CLNSRC
CLNACC RCV000171351.1,