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

rs1057518004

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518004(C;T)
Make rs1057518004(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position134842259
GeneCOL5A1, LOC101448202
is asnp
is mentioned by
dbSNPrs1057518004
dbSNP (old)rs1057518004
ClinGenrs1057518004
ebirs1057518004
HLIrs1057518004
Exacrs1057518004
Gnomadrs1057518004
Varsomers1057518004
LitVarrs1057518004
Maprs1057518004
PheGenIrs1057518004
Biobankrs1057518004
1000 genomesrs1057518004
hgdprs1057518004
ensemblrs1057518004
gopubmedrs1057518004
geneviewrs1057518004
scholarrs1057518004
googlers1057518004
pharmgkbrs1057518004
gwascentralrs1057518004
openSNPrs1057518004
23andMers1057518004
23andMe allrs1057518004
SNPshotrs1057518004
SNPdbers1057518004
MSV3drs1057518004
GWAS Ctlgrs1057518004
Max Magnitude0
ClinVar
Risk rs1057518004(T;T)
Alt rs1057518004(T;T)
Reference Rs1057518004(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL5A1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.137734105C>T
CLNSRC
CLNACC RCV000413639.1,