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rs794727573

From SNPedia

Orientationplus
Make rs794727573(-;-)
Make rs794727573(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2084637
GeneTSC2
is asnp
is mentioned by
dbSNPrs794727573
ebirs794727573
HLIrs794727573
Exacrs794727573
Varsomers794727573
Maprs794727573
PheGenIrs794727573
hapmaprs794727573
1000 genomesrs794727573
hgdprs794727573
ensemblrs794727573
gopubmedrs794727573
geneviewrs794727573
scholarrs794727573
googlers794727573
pharmgkbrs794727573
gwascentralrs794727573
openSNPrs794727573
23andMers794727573
23andMe allrs794727573
SNP Nexus

SNPshotrs794727573
SNPdbers794727573
MSV3drs794727573
GWAS Ctlgrs794727573
Max Magnitude
ClinVar
Risk rs794727573(;)
Alt rs794727573(;)
Reference rs794727573(G;G)
Significance Pathogenic
Disease Tuberous sclerosis 2
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis 2
Reversed 0
HGVS NC_000016.9:g.2134638delG
CLNSRC
CLNACC RCV000177762.1,