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rs1057518654

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518654(A;G)
Make rs1057518654(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position110172721
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs1057518654
dbSNP (old)rs1057518654
ClinGenrs1057518654
ebirs1057518654
HLIrs1057518654
Exacrs1057518654
Gnomadrs1057518654
Varsomers1057518654
Maprs1057518654
PheGenIrs1057518654
Biobankrs1057518654
1000 genomesrs1057518654
hgdprs1057518654
ensemblrs1057518654
gopubmedrs1057518654
geneviewrs1057518654
scholarrs1057518654
googlers1057518654
pharmgkbrs1057518654
gwascentralrs1057518654
openSNPrs1057518654
23andMers1057518654
23andMe allrs1057518654
SNPshotrs1057518654
SNPdbers1057518654
MSV3drs1057518654
GWAS Ctlgrs1057518654
Max Magnitude0
ClinVar
Risk rs1057518654(G;G)
Alt rs1057518654(G;G)
Reference Rs1057518654(A;A)
Significance Probable-Pathogenic
Disease Brain small vessel disease with hemorrhage
Variation info
Gene COL4A1
CLNDBN Brain small vessel disease with hemorrhage
Reversed 1
HGVS NC_000013.10:g.110825068T>C
CLNSRC
CLNACC RCV000414767.1,