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rs374020067

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374020067(C;T)
Make rs374020067(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position134732083
GeneCOL5A1
is asnp
is mentioned by
dbSNPrs374020067
ebirs374020067
HLIrs374020067
Exacrs374020067
Varsomers374020067
Maprs374020067
PheGenIrs374020067
hapmaprs374020067
1000 genomesrs374020067
hgdprs374020067
ensemblrs374020067
gopubmedrs374020067
geneviewrs374020067
scholarrs374020067
googlers374020067
pharmgkbrs374020067
gwascentralrs374020067
openSNPrs374020067
23andMers374020067
23andMe allrs374020067
SNP Nexus

SNPshotrs374020067
SNPdbers374020067
MSV3drs374020067
GWAS Ctlgrs374020067
Max Magnitude0
ClinVar
Risk rs374020067(T;T)
Alt rs374020067(T;T)
Reference rs374020067(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL5A1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.137623929C>T
CLNSRC
CLNACC RCV000197283.1,