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rs1057518103

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518103(C;C)
Make rs1057518103(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2088445
GenePKD1, TSC2
is asnp
is mentioned by
dbSNPrs1057518103
dbSNP (old)rs1057518103
ClinGenrs1057518103
ebirs1057518103
HLIrs1057518103
Exacrs1057518103
Gnomadrs1057518103
Varsomers1057518103
LitVarrs1057518103
Maprs1057518103
PheGenIrs1057518103
Biobankrs1057518103
1000 genomesrs1057518103
hgdprs1057518103
ensemblrs1057518103
gopubmedrs1057518103
geneviewrs1057518103
scholarrs1057518103
googlers1057518103
pharmgkbrs1057518103
gwascentralrs1057518103
openSNPrs1057518103
23andMers1057518103
23andMe allrs1057518103
SNPshotrs1057518103
SNPdbers1057518103
MSV3drs1057518103
GWAS Ctlgrs1057518103
Max Magnitude0
ClinVar
Risk rs1057518103(C;C)
Alt rs1057518103(C;C)
Reference Rs1057518103(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TSC2 PKD1
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2138446G>C
CLNSRC
CLNACC RCV000413128.1,