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rs796053516

From SNPedia

Orientationplus
Make rs796053516(-;-)
Make rs796053516(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2081720
GeneTSC2
is asnp
is mentioned by
dbSNPrs796053516
ebirs796053516
HLIrs796053516
Exacrs796053516
Varsomers796053516
Maprs796053516
PheGenIrs796053516
hapmaprs796053516
1000 genomesrs796053516
hgdprs796053516
ensemblrs796053516
gopubmedrs796053516
geneviewrs796053516
scholarrs796053516
googlers796053516
pharmgkbrs796053516
gwascentralrs796053516
openSNPrs796053516
23andMers796053516
23andMe allrs796053516
SNP Nexus

SNPshotrs796053516
SNPdbers796053516
MSV3drs796053516
GWAS Ctlgrs796053516
Max Magnitude
ClinVar
Risk rs796053516(;)
Alt rs796053516(;)
Reference rs796053516(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2131721delG
CLNSRC
CLNACC RCV000190085.1,