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rs773686174

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773686174(C;T)
Make rs773686174(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position46122147
GeneCOL6A2
is asnp
is mentioned by
dbSNPrs773686174
dbSNP (classic)rs773686174
ClinGenrs773686174
ebirs773686174
HLIrs773686174
Exacrs773686174
Gnomadrs773686174
Varsomers773686174
LitVarrs773686174
Maprs773686174
PheGenIrs773686174
Biobankrs773686174
1000 genomesrs773686174
hgdprs773686174
ensemblrs773686174
geneviewrs773686174
scholarrs773686174
googlers773686174
pharmgkbrs773686174
gwascentralrs773686174
openSNPrs773686174
23andMers773686174
SNPshotrs773686174
SNPdbers773686174
MSV3drs773686174
GWAS Ctlgrs773686174
Max Magnitude0
ClinVar
Risk rs773686174(T;T)
Alt rs773686174(T;T)
Reference Rs773686174(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL6A2
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.47542061C>T
CLNSRC
CLNACC RCV000481104.1,