rs755462817

Orientation

plus

Stabilized

plus

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

Make rs755462817(A;A)

Make rs755462817(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

218661852

Gene

BCS1L

is a	snp
is	mentioned by
dbSNP	rs755462817
dbSNP (classic)	rs755462817
ClinGen	rs755462817
ebi	rs755462817
HLI	rs755462817
Exac	rs755462817
Gnomad	rs755462817
Varsome	rs755462817
LitVar	rs755462817
Map	rs755462817
PheGenI	rs755462817
Biobank	rs755462817
1000 genomes	rs755462817
hgdp	rs755462817
ensembl	rs755462817
geneview	rs755462817
scholar	rs755462817
google	rs755462817
pharmgkb	rs755462817
gwascentral	rs755462817
openSNP	rs755462817
23andMe	rs755462817
SNPshot	rs755462817
SNPdbe	rs755462817
MSV3d	rs755462817
GWAS Ctlg	rs755462817

Max Magnitude

0

ClinVar
Risk	rs755462817(A;A)
Alt	rs755462817(A;A)
Reference	Rs755462817(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	BCS1L
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.219526575G>A
CLNSRC
CLNACC	RCV000197835.1,