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rs1060499710

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499710(A;A)
Make rs1060499710(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position108666550
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs1060499710
dbSNP (old)rs1060499710
ClinGenrs1060499710
ebirs1060499710
HLIrs1060499710
Exacrs1060499710
Gnomadrs1060499710
Varsomers1060499710
Maprs1060499710
PheGenIrs1060499710
Biobankrs1060499710
1000 genomesrs1060499710
hgdprs1060499710
ensemblrs1060499710
gopubmedrs1060499710
geneviewrs1060499710
scholarrs1060499710
googlers1060499710
pharmgkbrs1060499710
gwascentralrs1060499710
openSNPrs1060499710
23andMers1060499710
23andMe allrs1060499710
SNPshotrs1060499710
SNPdbers1060499710
MSV3drs1060499710
GWAS Ctlgrs1060499710
Max Magnitude0
ClinVar
Risk rs1060499710(A;A)
Alt rs1060499710(A;A)
Reference Rs1060499710(G;G)
Significance Probable-Pathogenic
Disease Alport syndrome
Variation info
Gene COL4A5
CLNDBN Alport syndrome, X-linked recessive
Reversed 0
HGVS NC_000023.10:g.107909780G>A
CLNSRC
CLNACC RCV000449531.1,