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rs759514548

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs759514548(G;T)
Make rs759514548(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position16000168
GeneTTC19, ZSWIM7
is asnp
is mentioned by
dbSNPrs759514548
ebirs759514548
HLIrs759514548
Exacrs759514548
Varsomers759514548
Maprs759514548
PheGenIrs759514548
hapmaprs759514548
1000 genomesrs759514548
hgdprs759514548
ensemblrs759514548
gopubmedrs759514548
geneviewrs759514548
scholarrs759514548
googlers759514548
pharmgkbrs759514548
gwascentralrs759514548
openSNPrs759514548
23andMers759514548
23andMe allrs759514548
SNP Nexus

SNPshotrs759514548
SNPdbers759514548
MSV3drs759514548
GWAS Ctlgrs759514548
Max Magnitude0
ClinVar
Risk rs759514548(T;T)
Alt rs759514548(T;T)
Reference rs759514548(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTC19 ZSWIM7
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.15903482G>T
CLNSRC
CLNACC RCV000200180.1,