rs748659198

Orientation

plus

Stabilized

plus

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

Make rs748659198(C;T)

Make rs748659198(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

235759159

Gene

LYST

is a	snp
is	mentioned by
dbSNP	rs748659198
dbSNP (classic)	rs748659198
ClinGen	rs748659198
ebi	rs748659198
HLI	rs748659198
Exac	rs748659198
Gnomad	rs748659198
Varsome	rs748659198
LitVar	rs748659198
Map	rs748659198
PheGenI	rs748659198
Biobank	rs748659198
1000 genomes	rs748659198
hgdp	rs748659198
ensembl	rs748659198
geneview	rs748659198
scholar	rs748659198
google	rs748659198
pharmgkb	rs748659198
gwascentral	rs748659198
openSNP	rs748659198
23andMe	rs748659198
SNPshot	rs748659198
SNPdbe	rs748659198
MSV3d	rs748659198
GWAS Ctlg	rs748659198

Max Magnitude

0

ClinVar
Risk	rs748659198(A;A) rs748659198(T;T)
Alt	rs748659198(A;A) rs748659198(T;T)
Reference	Rs748659198(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LYST
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.235922459C>A
CLNSRC
CLNACC	RCV000171169.1,