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rs201868387

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201868387(A;A)
Make rs201868387(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position24260026
GeneTGM1
is asnp
is mentioned by
dbSNPrs201868387
dbSNP (old)rs201868387
ClinGenrs201868387
ebirs201868387
HLIrs201868387
Exacrs201868387
Gnomadrs201868387
Varsomers201868387
Maprs201868387
PheGenIrs201868387
Biobankrs201868387
1000 genomesrs201868387
hgdprs201868387
ensemblrs201868387
gopubmedrs201868387
geneviewrs201868387
scholarrs201868387
googlers201868387
pharmgkbrs201868387
gwascentralrs201868387
openSNPrs201868387
23andMers201868387
23andMe allrs201868387
SNPshotrs201868387
SNPdbers201868387
MSV3drs201868387
GWAS Ctlgrs201868387
Max Magnitude0
ClinVar
Risk rs201868387(A;A)
Alt rs201868387(A;A)
Reference Rs201868387(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TGM1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.24729232G>A
CLNSRC
CLNACC RCV000413495.1,