rs863223915

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AT;AT)	0	common in clinvar
(I;I)	0	common genotype

Make rs863223915(-;-)

Make rs863223915(-;AT)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

218661923

Gene

BCS1L

is a	snp
is	mentioned by
dbSNP	rs863223915
dbSNP (classic)	rs863223915
ClinGen	rs863223915
ebi	rs863223915
HLI	rs863223915
Exac	rs863223915
Gnomad	rs863223915
Varsome	rs863223915
LitVar	rs863223915
Map	rs863223915
PheGenI	rs863223915
Biobank	rs863223915
1000 genomes	rs863223915
hgdp	rs863223915
ensembl	rs863223915
geneview	rs863223915
scholar	rs863223915
google	rs863223915
pharmgkb	rs863223915
gwascentral	rs863223915
openSNP	rs863223915
23andMe	rs863223915
SNPshot	rs863223915
SNPdbe	rs863223915
MSV3d	rs863223915
GWAS Ctlg	rs863223915

Max Magnitude

0

ClinVar
Risk	rs863223915(-;-)
Alt	rs863223915(-;-)
Reference	Rs863223915(AT;AT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	BCS1L
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.219526646_219526647delAT
CLNSRC
CLNACC	RCV000199046.1,