rs898673491

Orientation

plus

Stabilized

plus

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

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

7025974

Gene

LAMA1

is a	snp
is	mentioned by
dbSNP	rs898673491
dbSNP (classic)	rs898673491
ClinGen	rs898673491
ebi	rs898673491
HLI	rs898673491
Exac	rs898673491
Gnomad	rs898673491
Varsome	rs898673491
LitVar	rs898673491
Map	rs898673491
PheGenI	rs898673491
Biobank	rs898673491
1000 genomes	rs898673491
hgdp	rs898673491
ensembl	rs898673491
geneview	rs898673491
scholar	rs898673491
google	rs898673491
pharmgkb	rs898673491
gwascentral	rs898673491
openSNP	rs898673491
23andMe	rs898673491
SNPshot	rs898673491
SNPdbe	rs898673491
MSV3d	rs898673491
GWAS Ctlg	rs898673491

Max Magnitude

0

ClinVar
Risk	rs898673491(T;T)
Alt	rs898673491(T;T)
Reference	Rs898673491(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.7025973C>T
CLNSRC
CLNACC	RCV000494106.1,