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rs1057519090

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519090(A;A)
Make rs1057519090(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position110492105
GeneCOL4A2
is asnp
is mentioned by
dbSNPrs1057519090
dbSNP (old)rs1057519090
ClinGenrs1057519090
ebirs1057519090
HLIrs1057519090
Exacrs1057519090
Gnomadrs1057519090
Varsomers1057519090
LitVarrs1057519090
Maprs1057519090
PheGenIrs1057519090
Biobankrs1057519090
1000 genomesrs1057519090
hgdprs1057519090
ensemblrs1057519090
gopubmedrs1057519090
geneviewrs1057519090
scholarrs1057519090
googlers1057519090
pharmgkbrs1057519090
gwascentralrs1057519090
openSNPrs1057519090
23andMers1057519090
23andMe allrs1057519090
SNPshotrs1057519090
SNPdbers1057519090
MSV3drs1057519090
GWAS Ctlgrs1057519090
Max Magnitude0
ClinVar
Risk rs1057519090(A;A)
Alt rs1057519090(A;A)
Reference Rs1057519090(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL4A2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.111144452G>A
CLNSRC
CLNACC RCV000416075.1,