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

rs1057518100

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518100(A;A)
Make rs1057518100(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position110169708
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs1057518100
dbSNP (old)rs1057518100
ClinGenrs1057518100
ebirs1057518100
HLIrs1057518100
Exacrs1057518100
Gnomadrs1057518100
Varsomers1057518100
Maprs1057518100
PheGenIrs1057518100
Biobankrs1057518100
1000 genomesrs1057518100
hgdprs1057518100
ensemblrs1057518100
gopubmedrs1057518100
geneviewrs1057518100
scholarrs1057518100
googlers1057518100
pharmgkbrs1057518100
gwascentralrs1057518100
openSNPrs1057518100
23andMers1057518100
23andMe allrs1057518100
SNP Nexus

SNPshotrs1057518100
SNPdbers1057518100
MSV3drs1057518100
GWAS Ctlgrs1057518100
Max Magnitude0
ClinVar
Risk rs1057518100(A;A)
Alt rs1057518100(A;A)
Reference Rs1057518100(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL4A1
CLNDBN not provided
Reversed 1
HGVS NC_000013.10:g.110822055C>T
CLNSRC
CLNACC RCV000414372.1,