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rs1057518959

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518959(C;C)
Make rs1057518959(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2091794
GeneLOC105371049, MIR1225, PKD1
is asnp
is mentioned by
dbSNPrs1057518959
dbSNP (old)rs1057518959
ClinGenrs1057518959
ebirs1057518959
HLIrs1057518959
Exacrs1057518959
Gnomadrs1057518959
Varsomers1057518959
Maprs1057518959
PheGenIrs1057518959
Biobankrs1057518959
1000 genomesrs1057518959
hgdprs1057518959
ensemblrs1057518959
gopubmedrs1057518959
geneviewrs1057518959
scholarrs1057518959
googlers1057518959
pharmgkbrs1057518959
gwascentralrs1057518959
openSNPrs1057518959
23andMers1057518959
23andMe allrs1057518959
SNPshotrs1057518959
SNPdbers1057518959
MSV3drs1057518959
GWAS Ctlgrs1057518959
Max Magnitude0
ClinVar
Risk rs1057518959(C;C)
Alt rs1057518959(C;C)
Reference Rs1057518959(T;T)
Significance Probable-Pathogenic
Disease Hypertension Polycystic kidney dysplasia
Variation info
Gene PKD1 MIR1225 LOC105371049
CLNDBN Hypertension Polycystic kidney dysplasia
Reversed 1
HGVS NC_000016.9:g.2141795A>G
CLNSRC
CLNACC RCV000415211.1,