rs797045900

Orientation

plus

Stabilized

plus

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

Make rs797045900(A;A)

Make rs797045900(A;T)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

53882648

Gene

PRKCG

is a	snp
is	mentioned by
dbSNP	rs797045900
dbSNP (classic)	rs797045900
ClinGen	rs797045900
ebi	rs797045900
HLI	rs797045900
Exac	rs797045900
Gnomad	rs797045900
Varsome	rs797045900
LitVar	rs797045900
Map	rs797045900
PheGenI	rs797045900
Biobank	rs797045900
1000 genomes	rs797045900
hgdp	rs797045900
ensembl	rs797045900
geneview	rs797045900
scholar	rs797045900
google	rs797045900
pharmgkb	rs797045900
gwascentral	rs797045900
openSNP	rs797045900
23andMe	rs797045900
SNPshot	rs797045900
SNPdbe	rs797045900
MSV3d	rs797045900
GWAS Ctlg	rs797045900

Max Magnitude

0

ClinVar
Risk	rs797045900(A;A)
Alt	rs797045900(A;A)
Reference	Rs797045900(T;T)
Significance	Probable-Pathogenic
Disease	Spinocerebellar ataxia 14
Variation	info
Gene	PRKCG
CLNDBN	Spinocerebellar ataxia 14
Reversed	0
HGVS	NC_000019.9:g.54385902T>A
CLNSRC
CLNACC	RCV000194843.1,