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rs192522753

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs192522753(C;T)
Make rs192522753(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position16027376
GeneTTC19
is asnp
is mentioned by
dbSNPrs192522753
ebirs192522753
HLIrs192522753
Exacrs192522753
Varsomers192522753
Maprs192522753
PheGenIrs192522753
hapmaprs192522753
1000 genomesrs192522753
hgdprs192522753
ensemblrs192522753
gopubmedrs192522753
geneviewrs192522753
scholarrs192522753
googlers192522753
pharmgkbrs192522753
gwascentralrs192522753
openSNPrs192522753
23andMers192522753
23andMe allrs192522753
SNP Nexus

SNPshotrs192522753
SNPdbers192522753
MSV3drs192522753
GWAS Ctlgrs192522753
Max Magnitude0
ClinVar
Risk rs192522753(A,T;A,T)
Alt rs192522753(A,T;A,T)
Reference rs192522753(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene TTC19
CLNDBN not specified
Reversed 0
HGVS NC_000017.10:g.15930690C>T
CLNSRC
CLNACC RCV000196721.2,