rs1057519098

Orientation

plus

Stabilized

plus

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

Make rs1057519098(-;-)

Make rs1057519098(-;AG)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

11753639

Gene

GNAL

is a	snp
is	mentioned by
dbSNP	rs1057519098
dbSNP (classic)	rs1057519098
ClinGen	rs1057519098
ebi	rs1057519098
HLI	rs1057519098
Exac	rs1057519098
Gnomad	rs1057519098
Varsome	rs1057519098
LitVar	rs1057519098
Map	rs1057519098
PheGenI	rs1057519098
Biobank	rs1057519098
1000 genomes	rs1057519098
hgdp	rs1057519098
ensembl	rs1057519098
geneview	rs1057519098
scholar	rs1057519098
google	rs1057519098
pharmgkb	rs1057519098
gwascentral	rs1057519098
openSNP	rs1057519098
23andMe	rs1057519098
SNPshot	rs1057519098
SNPdbe	rs1057519098
MSV3d	rs1057519098
GWAS Ctlg	rs1057519098

Max Magnitude

0

ClinVar
Risk	rs1057519098(-;-)
Alt	rs1057519098(-;-)
Reference	Rs1057519098(AG;AG)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GNAL
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.11753638_11753639delAG
CLNSRC
CLNACC	RCV000416229.1,