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rs1060499676

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499676(C;G)
Make rs1060499676(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2088234
GenePKD1, TSC2
is asnp
is mentioned by
dbSNPrs1060499676
dbSNP (old)rs1060499676
ClinGenrs1060499676
ebirs1060499676
HLIrs1060499676
Exacrs1060499676
Gnomadrs1060499676
Varsomers1060499676
Maprs1060499676
PheGenIrs1060499676
Biobankrs1060499676
1000 genomesrs1060499676
hgdprs1060499676
ensemblrs1060499676
gopubmedrs1060499676
geneviewrs1060499676
scholarrs1060499676
googlers1060499676
pharmgkbrs1060499676
gwascentralrs1060499676
openSNPrs1060499676
23andMers1060499676
23andMe allrs1060499676
SNPshotrs1060499676
SNPdbers1060499676
MSV3drs1060499676
GWAS Ctlgrs1060499676
Max Magnitude0
ClinVar
Risk rs1060499676(G;G)
Alt rs1060499676(G;G)
Reference Rs1060499676(C;C)
Significance Pathogenic
Disease Tuberous sclerosis 2
Variation info
Gene TSC2 PKD1
CLNDBN Tuberous sclerosis 2
Reversed 0
HGVS NC_000016.9:g.2138235C>G
CLNSRC
CLNACC RCV000449506.1,