rs776158594

Orientation

plus

Stabilized

plus

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

Make rs776158594(A;G)

Make rs776158594(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

22

Position

50580356

Gene	CHKB, CHKB-CPT1B, CPT1B

is a	snp
is	mentioned by
dbSNP	rs776158594
dbSNP (classic)	rs776158594
ClinGen	rs776158594
ebi	rs776158594
HLI	rs776158594
Exac	rs776158594
Gnomad	rs776158594
Varsome	rs776158594
LitVar	rs776158594
Map	rs776158594
PheGenI	rs776158594
Biobank	rs776158594
1000 genomes	rs776158594
hgdp	rs776158594
ensembl	rs776158594
geneview	rs776158594
scholar	rs776158594
google	rs776158594
pharmgkb	rs776158594
gwascentral	rs776158594
openSNP	rs776158594
23andMe	rs776158594
SNPshot	rs776158594
SNPdbe	rs776158594
MSV3d	rs776158594
GWAS Ctlg	rs776158594

Max Magnitude

0

ClinVar
Risk	rs776158594(G;G)
Alt	rs776158594(G;G)
Reference	Rs776158594(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CHKB-CPT1B CHKB CPT1B
CLNDBN	not provided
Reversed	0
HGVS	NC_000022.10:g.51018785A>G
CLNSRC
CLNACC	RCV000494588.1,