rs771599779

Orientation

plus

Stabilized

plus

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

Make rs771599779(A;A)

Make rs771599779(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

47996909

Gene

SUCLA2

is a	snp
is	mentioned by
dbSNP	rs771599779
dbSNP (classic)	rs771599779
ClinGen	rs771599779
ebi	rs771599779
HLI	rs771599779
Exac	rs771599779
Gnomad	rs771599779
Varsome	rs771599779
LitVar	rs771599779
Map	rs771599779
PheGenI	rs771599779
Biobank	rs771599779
1000 genomes	rs771599779
hgdp	rs771599779
ensembl	rs771599779
geneview	rs771599779
scholar	rs771599779
google	rs771599779
pharmgkb	rs771599779
gwascentral	rs771599779
openSNP	rs771599779
23andMe	rs771599779
SNPshot	rs771599779
SNPdbe	rs771599779
MSV3d	rs771599779
GWAS Ctlg	rs771599779

Max Magnitude

0

ClinVar
Risk	rs771599779(A;A)
Alt	rs771599779(A;A)
Reference	Rs771599779(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SUCLA2
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.48571044C>A
CLNSRC
CLNACC	RCV000186189.1,