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rs769078093

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs769078093(G;T)
Make rs769078093(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position15999807
GeneTTC19, ZSWIM7
is asnp
is mentioned by
dbSNPrs769078093
ebirs769078093
HLIrs769078093
Exacrs769078093
Varsomers769078093
Maprs769078093
PheGenIrs769078093
hapmaprs769078093
1000 genomesrs769078093
hgdprs769078093
ensemblrs769078093
gopubmedrs769078093
geneviewrs769078093
scholarrs769078093
googlers769078093
pharmgkbrs769078093
gwascentralrs769078093
openSNPrs769078093
23andMers769078093
23andMe allrs769078093
SNP Nexus

SNPshotrs769078093
SNPdbers769078093
MSV3drs769078093
GWAS Ctlgrs769078093
Max Magnitude0
ClinVar
Risk rs769078093(A,T;A,T)
Alt rs769078093(A,T;A,T)
Reference rs769078093(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTC19 ZSWIM7
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.15903121G>T
CLNSRC
CLNACC RCV000196528.2,