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

rs760446904

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs760446904(C;T)
Make rs760446904(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position237361132
GeneCOL6A3
is asnp
is mentioned by
dbSNPrs760446904
dbSNP (classic)rs760446904
ClinGenrs760446904
ebirs760446904
HLIrs760446904
Exacrs760446904
Gnomadrs760446904
Varsomers760446904
LitVarrs760446904
Maprs760446904
PheGenIrs760446904
Biobankrs760446904
1000 genomesrs760446904
hgdprs760446904
ensemblrs760446904
geneviewrs760446904
scholarrs760446904
googlers760446904
pharmgkbrs760446904
gwascentralrs760446904
openSNPrs760446904
23andMers760446904
23andMe allrs760446904
SNPshotrs760446904
SNPdbers760446904
MSV3drs760446904
GWAS Ctlgrs760446904
Max Magnitude0
ClinVar
Risk rs760446904(T;T)
Alt rs760446904(T;T)
Reference Rs760446904(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene COL6A3
CLNDBN not specified not provided
Reversed 0
HGVS NC_000002.11:g.238269775C>T
CLNSRC
CLNACC RCV000274706.1, RCV000494333.1,