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rs201677741

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201677741(G;T)
Make rs201677741(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position24240544
GeneTINF2
is asnp
is mentioned by
dbSNPrs201677741
dbSNP (old)rs201677741
ClinGenrs201677741
ebirs201677741
HLIrs201677741
Exacrs201677741
Gnomadrs201677741
Varsomers201677741
Maprs201677741
PheGenIrs201677741
Biobankrs201677741
1000 genomesrs201677741
hgdprs201677741
ensemblrs201677741
gopubmedrs201677741
geneviewrs201677741
scholarrs201677741
googlers201677741
pharmgkbrs201677741
gwascentralrs201677741
openSNPrs201677741
23andMers201677741
23andMe allrs201677741
SNPshotrs201677741
SNPdbers201677741
MSV3drs201677741
GWAS Ctlgrs201677741
Max Magnitude0
ClinVar
Risk rs201677741(T;T)
Alt rs201677741(T;T)
Reference Rs201677741(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TINF2
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.24709750G>T
CLNSRC
CLNACC RCV000400895.1,