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rs1057523764

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523764(A;A)
Make rs1057523764(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position110465526
GeneCOL4A2
is asnp
is mentioned by
dbSNPrs1057523764
dbSNP (old)rs1057523764
ClinGenrs1057523764
ebirs1057523764
HLIrs1057523764
Exacrs1057523764
Gnomadrs1057523764
Varsomers1057523764
Maprs1057523764
PheGenIrs1057523764
Biobankrs1057523764
1000 genomesrs1057523764
hgdprs1057523764
ensemblrs1057523764
gopubmedrs1057523764
geneviewrs1057523764
scholarrs1057523764
googlers1057523764
pharmgkbrs1057523764
gwascentralrs1057523764
openSNPrs1057523764
23andMers1057523764
23andMe allrs1057523764
SNPshotrs1057523764
SNPdbers1057523764
MSV3drs1057523764
GWAS Ctlgrs1057523764
Max Magnitude0
ClinVar
Risk rs1057523764(A;A)
Alt rs1057523764(A;A)
Reference Rs1057523764(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL4A2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.111117873G>A
CLNSRC
CLNACC RCV000426149.1,