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rs779592523

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs779592523(A;A)
Make rs779592523(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position16000127
GeneTTC19, ZSWIM7
is asnp
is mentioned by
dbSNPrs779592523
ebirs779592523
HLIrs779592523
Exacrs779592523
Varsomers779592523
Maprs779592523
PheGenIrs779592523
hapmaprs779592523
1000 genomesrs779592523
hgdprs779592523
ensemblrs779592523
gopubmedrs779592523
geneviewrs779592523
scholarrs779592523
googlers779592523
pharmgkbrs779592523
gwascentralrs779592523
openSNPrs779592523
23andMers779592523
23andMe allrs779592523
SNP Nexus

SNPshotrs779592523
SNPdbers779592523
MSV3drs779592523
GWAS Ctlgrs779592523
Max Magnitude0
ClinVar
Risk rs779592523(A,C;A,C)
Alt rs779592523(A,C;A,C)
Reference rs779592523(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTC19 ZSWIM7
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.15903441G>A
CLNSRC
CLNACC RCV000197613.1,