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rs1057518125

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518125(G;T)
Make rs1057518125(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position108666531
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs1057518125
dbSNP (old)rs1057518125
ClinGenrs1057518125
ebirs1057518125
HLIrs1057518125
Exacrs1057518125
Gnomadrs1057518125
Varsomers1057518125
Maprs1057518125
PheGenIrs1057518125
Biobankrs1057518125
1000 genomesrs1057518125
hgdprs1057518125
ensemblrs1057518125
gopubmedrs1057518125
geneviewrs1057518125
scholarrs1057518125
googlers1057518125
pharmgkbrs1057518125
gwascentralrs1057518125
openSNPrs1057518125
23andMers1057518125
23andMe allrs1057518125
SNPshotrs1057518125
SNPdbers1057518125
MSV3drs1057518125
GWAS Ctlgrs1057518125
Max Magnitude0
ClinVar
Risk rs1057518125(T;T)
Alt rs1057518125(T;T)
Reference Rs1057518125(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL4A5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.107909761G>T
CLNSRC
CLNACC RCV000412740.1,