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rs137854071

From SNPedia

Orientationplus
Make rs137854071(-;-)
Make rs137854071(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2071908
GeneTSC2
is asnp
is mentioned by
dbSNPrs137854071
ebirs137854071
HLIrs137854071
Exacrs137854071
Varsomers137854071
Maprs137854071
PheGenIrs137854071
hapmaprs137854071
1000 genomesrs137854071
hgdprs137854071
ensemblrs137854071
gopubmedrs137854071
geneviewrs137854071
scholarrs137854071
googlers137854071
pharmgkbrs137854071
gwascentralrs137854071
openSNPrs137854071
23andMers137854071
23andMe allrs137854071
SNP Nexus

SNPshotrs137854071
SNPdbers137854071
MSV3drs137854071
GWAS Ctlgrs137854071
Max Magnitude
ClinVar
Risk rs137854071(;)
Alt rs137854071(;)
Reference rs137854071(C;C)
Significance Pathogenic
Disease Tuberous sclerosis syndrome not provided
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis syndrome not provided
Reversed 0
HGVS NC_000016.9:g.2121909delC
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000042979.2, RCV000190058.1,