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rs45491698

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45491698(C;C)
Make rs45491698(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2079160
GeneTSC2
is asnp
is mentioned by
dbSNPrs45491698
ebirs45491698
HLIrs45491698
Exacrs45491698
Varsomers45491698
Maprs45491698
PheGenIrs45491698
hapmaprs45491698
1000 genomesrs45491698
hgdprs45491698
ensemblrs45491698
gopubmedrs45491698
geneviewrs45491698
scholarrs45491698
googlers45491698
pharmgkbrs45491698
gwascentralrs45491698
openSNPrs45491698
23andMers45491698
23andMe allrs45491698
SNP Nexus

SNPshotrs45491698
SNPdbers45491698
MSV3drs45491698
GWAS Ctlgrs45491698
Max Magnitude0
ClinVar
Risk rs45491698(A,C;A,C)
Alt rs45491698(A,C;A,C)
Reference rs45491698(G;G)
Significance Probable-Pathogenic
Disease Tuberous sclerosis syndrome Tuberous sclerosis 2
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis syndrome Tuberous sclerosis 2
Reversed 0
HGVS NC_000016.9:g.2129161G>C
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000042500.2, RCV000201071.1,