rs730880295

Orientation

plus

Stabilized

plus

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

Make rs730880295(C;C)

Make rs730880295(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

43883879

Gene

LACC1

is a	snp
is	mentioned by
dbSNP	rs730880295
dbSNP (classic)	rs730880295
ClinGen	rs730880295
ebi	rs730880295
HLI	rs730880295
Exac	rs730880295
Gnomad	rs730880295
Varsome	rs730880295
LitVar	rs730880295
Map	rs730880295
PheGenI	rs730880295
Biobank	rs730880295
1000 genomes	rs730880295
hgdp	rs730880295
ensembl	rs730880295
geneview	rs730880295
scholar	rs730880295
google	rs730880295
pharmgkb	rs730880295
gwascentral	rs730880295
openSNP	rs730880295
23andMe	rs730880295
SNPshot	rs730880295
SNPdbe	rs730880295
MSV3d	rs730880295
GWAS Ctlg	rs730880295

Max Magnitude

0

ClinVar
Risk	rs730880295(C;C)
Alt	rs730880295(C;C)
Reference	Rs730880295(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LACC1
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.44458015T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000157633.4, RCV000171123.1,