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

rs1057517719

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517719(C;T)
Make rs1057517719(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position110205367
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs1057517719
dbSNP (classic)rs1057517719
ClinGenrs1057517719
ebirs1057517719
HLIrs1057517719
Exacrs1057517719
Gnomadrs1057517719
Varsomers1057517719
LitVarrs1057517719
Maprs1057517719
PheGenIrs1057517719
Biobankrs1057517719
1000 genomesrs1057517719
hgdprs1057517719
ensemblrs1057517719
geneviewrs1057517719
scholarrs1057517719
googlers1057517719
pharmgkbrs1057517719
gwascentralrs1057517719
openSNPrs1057517719
23andMers1057517719
SNPshotrs1057517719
SNPdbers1057517719
MSV3drs1057517719
GWAS Ctlgrs1057517719
Max Magnitude0
ClinVar
Risk rs1057517719(T;T)
Alt rs1057517719(T;T)
Reference Rs1057517719(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL4A1
CLNDBN not provided
Reversed 1
HGVS NC_000013.10:g.110857714G>A
CLNSRC
CLNACC RCV000414476.1,