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rs796053507

From SNPedia

Orientationplus
Make rs796053507(-;-)
Make rs796053507(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2088448
GenePKD1, TSC2
is asnp
is mentioned by
dbSNPrs796053507
ebirs796053507
HLIrs796053507
Exacrs796053507
Varsomers796053507
Maprs796053507
PheGenIrs796053507
hapmaprs796053507
1000 genomesrs796053507
hgdprs796053507
ensemblrs796053507
gopubmedrs796053507
geneviewrs796053507
scholarrs796053507
googlers796053507
pharmgkbrs796053507
gwascentralrs796053507
openSNPrs796053507
23andMers796053507
23andMe allrs796053507
SNP Nexus

SNPshotrs796053507
SNPdbers796053507
MSV3drs796053507
GWAS Ctlgrs796053507
Max Magnitude
ClinVar
Risk rs796053507(;)
Alt rs796053507(;)
Reference rs796053507(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2 PKD1
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2138449delC
CLNSRC
CLNACC RCV000190064.1,