rs192522753

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs192522753(C;T)

Make rs192522753(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

16027376

Gene

TTC19

is a	snp
is	mentioned by
dbSNP	rs192522753
dbSNP (classic)	rs192522753
ClinGen	rs192522753
ebi	rs192522753
HLI	rs192522753
Exac	rs192522753
Gnomad	rs192522753
Varsome	rs192522753
LitVar	rs192522753
Map	rs192522753
PheGenI	rs192522753
Biobank	rs192522753
1000 genomes	rs192522753
hgdp	rs192522753
ensembl	rs192522753
geneview	rs192522753
scholar	rs192522753
google	rs192522753
pharmgkb	rs192522753
gwascentral	rs192522753
openSNP	rs192522753
23andMe	rs192522753
SNPshot	rs192522753
SNPdbe	rs192522753
MSV3d	rs192522753
GWAS Ctlg	rs192522753

Max Magnitude

0

ClinVar
Risk	rs192522753(A;A) rs192522753(T;T)
Alt	rs192522753(A;A) rs192522753(T;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,