rs864309643

Orientation

plus

Stabilized

plus

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

Make rs864309643(A;A)

Make rs864309643(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

45516144

Gene

LARS2

is a	snp
is	mentioned by
dbSNP	rs864309643
dbSNP (classic)	rs864309643
ClinGen	rs864309643
ebi	rs864309643
HLI	rs864309643
Exac	rs864309643
Gnomad	rs864309643
Varsome	rs864309643
LitVar	rs864309643
Map	rs864309643
PheGenI	rs864309643
Biobank	rs864309643
1000 genomes	rs864309643
hgdp	rs864309643
ensembl	rs864309643
geneview	rs864309643
scholar	rs864309643
google	rs864309643
pharmgkb	rs864309643
gwascentral	rs864309643
openSNP	rs864309643
23andMe	rs864309643
SNPshot	rs864309643
SNPdbe	rs864309643
MSV3d	rs864309643
GWAS Ctlg	rs864309643

Max Magnitude

0

ClinVar
Risk	rs864309643(A;A)
Alt	rs864309643(A;A)
Reference	Rs864309643(G;G)
Significance	Pathogenic
Disease	Perrault syndrome 4
Variation	info
Gene	LARS2
CLNDBN	Perrault syndrome 4
Reversed	0
HGVS	NC_000003.11:g.45557636G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000203255.2, RCV000203256.1,