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rs796053515

From SNPedia

Orientationplus
Make rs796053515(-;-)
Make rs796053515(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2048647
GeneNTHL1, TSC2
is asnp
is mentioned by
dbSNPrs796053515
ClinGenrs796053515
ebirs796053515
HLIrs796053515
Exacrs796053515
Varsomers796053515
Maprs796053515
PheGenIrs796053515
hapmaprs796053515
1000 genomesrs796053515
hgdprs796053515
ensemblrs796053515
gopubmedrs796053515
geneviewrs796053515
scholarrs796053515
googlers796053515
pharmgkbrs796053515
gwascentralrs796053515
openSNPrs796053515
23andMers796053515
23andMe allrs796053515
SNP Nexus

SNPshotrs796053515
SNPdbers796053515
MSV3drs796053515
GWAS Ctlgrs796053515
Max Magnitude
ClinVar
Risk
Alt
Reference Rs796053515(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene NTHL1 TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2098648delT
CLNSRC
CLNACC RCV000190084.1,