rs876661247

Orientation

plus

Stabilized

plus

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

Make rs876661247(C;T)

Make rs876661247(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

127501108

Gene

LRSAM1

is a	snp
is	mentioned by
dbSNP	rs876661247
dbSNP (classic)	rs876661247
ClinGen	rs876661247
ebi	rs876661247
HLI	rs876661247
Exac	rs876661247
Gnomad	rs876661247
Varsome	rs876661247
LitVar	rs876661247
Map	rs876661247
PheGenI	rs876661247
Biobank	rs876661247
1000 genomes	rs876661247
hgdp	rs876661247
ensembl	rs876661247
geneview	rs876661247
scholar	rs876661247
google	rs876661247
pharmgkb	rs876661247
gwascentral	rs876661247
openSNP	rs876661247
23andMe	rs876661247
SNPshot	rs876661247
SNPdbe	rs876661247
MSV3d	rs876661247
GWAS Ctlg	rs876661247

Max Magnitude

0

ClinVar
Risk	rs876661247(T;T)
Alt	rs876661247(T;T)
Reference	Rs876661247(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LRSAM1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.130263387C>T
CLNSRC
CLNACC	RCV000214671.1,