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rs587778004

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778004(G;T)
Make rs587778004(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2048066
GeneNTHL1, TSC2
is asnp
is mentioned by
dbSNPrs587778004
ebirs587778004
HLIrs587778004
Exacrs587778004
Varsomers587778004
Maprs587778004
PheGenIrs587778004
hapmaprs587778004
1000 genomesrs587778004
hgdprs587778004
ensemblrs587778004
gopubmedrs587778004
geneviewrs587778004
scholarrs587778004
googlers587778004
pharmgkbrs587778004
gwascentralrs587778004
openSNPrs587778004
23andMers587778004
23andMe allrs587778004
SNP Nexus

SNPshotrs587778004
SNPdbers587778004
MSV3drs587778004
GWAS Ctlgrs587778004
Max Magnitude0
ClinVar
Risk rs587778004(C,T;C,T)
Alt rs587778004(C,T;C,T)
Reference rs587778004(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene NTHL1 TSC2
CLNDBN not provided not specified
Reversed 0
HGVS NC_000016.9:g.2098067G>C; NC_000016.9:g.2098067G>T
CLNSRC
CLNACC RCV000190049.2, RCV000119926.2,