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rs756830714

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756830714(C;T)
Make rs756830714(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position15999855
GeneTTC19, ZSWIM7
is asnp
is mentioned by
dbSNPrs756830714
ebirs756830714
HLIrs756830714
Exacrs756830714
Varsomers756830714
Maprs756830714
PheGenIrs756830714
hapmaprs756830714
1000 genomesrs756830714
hgdprs756830714
ensemblrs756830714
gopubmedrs756830714
geneviewrs756830714
scholarrs756830714
googlers756830714
pharmgkbrs756830714
gwascentralrs756830714
openSNPrs756830714
23andMers756830714
23andMe allrs756830714
SNP Nexus

SNPshotrs756830714
SNPdbers756830714
MSV3drs756830714
GWAS Ctlgrs756830714
Max Magnitude0
ClinVar
Risk rs756830714(T;T)
Alt rs756830714(T;T)
Reference rs756830714(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTC19 ZSWIM7
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.15903169C>T
CLNSRC
CLNACC RCV000197767.1,