rs797044940

Orientation

minus

Stabilized

minus

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

Make rs797044940(C;C)

Make rs797044940(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

6958571

Gene

LAMA1

is a	snp
is	mentioned by
dbSNP	rs797044940
dbSNP (classic)	rs797044940
ClinGen	rs797044940
ebi	rs797044940
HLI	rs797044940
Exac	rs797044940
Gnomad	rs797044940
Varsome	rs797044940
LitVar	rs797044940
Map	rs797044940
PheGenI	rs797044940
Biobank	rs797044940
1000 genomes	rs797044940
hgdp	rs797044940
ensembl	rs797044940
geneview	rs797044940
scholar	rs797044940
google	rs797044940
pharmgkb	rs797044940
gwascentral	rs797044940
openSNP	rs797044940
23andMe	rs797044940
SNPshot	rs797044940
SNPdbe	rs797044940
MSV3d	rs797044940
GWAS Ctlg	rs797044940

Max Magnitude

0

ClinVar
Risk	rs797044940(C;C)
Alt	rs797044940(C;C)
Reference	Rs797044940(T;T)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	LAMA1
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000018.9:g.6958570A>G
CLNSRC
CLNACC	RCV000190786.1,