rs797044926

Orientation

minus

Stabilized

minus

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

Make rs797044926(A;A)

Make rs797044926(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

65523578

Gene

LAS1L

is a	snp
is	mentioned by
dbSNP	rs797044926
dbSNP (classic)	rs797044926
ClinGen	rs797044926
ebi	rs797044926
HLI	rs797044926
Exac	rs797044926
Gnomad	rs797044926
Varsome	rs797044926
LitVar	rs797044926
Map	rs797044926
PheGenI	rs797044926
Biobank	rs797044926
1000 genomes	rs797044926
hgdp	rs797044926
ensembl	rs797044926
geneview	rs797044926
scholar	rs797044926
google	rs797044926
pharmgkb	rs797044926
gwascentral	rs797044926
openSNP	rs797044926
23andMe	rs797044926
SNPshot	rs797044926
SNPdbe	rs797044926
MSV3d	rs797044926
GWAS Ctlg	rs797044926

Max Magnitude

0

ClinVar
Risk	rs797044926(A;A)
Alt	rs797044926(A;A)
Reference	Rs797044926(G;G)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	LAS1L
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000023.10:g.64743458C>T
CLNSRC
CLNACC	RCV000190764.1,