rs757905943

Orientation

plus

Stabilized

plus

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

Make rs757905943(A;A)

Make rs757905943(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

89101029

Gene

ACSF3

is a	snp
is	mentioned by
dbSNP	rs757905943
dbSNP (classic)	rs757905943
ClinGen	rs757905943
ebi	rs757905943
HLI	rs757905943
Exac	rs757905943
Gnomad	rs757905943
Varsome	rs757905943
LitVar	rs757905943
Map	rs757905943
PheGenI	rs757905943
Biobank	rs757905943
1000 genomes	rs757905943
hgdp	rs757905943
ensembl	rs757905943
geneview	rs757905943
scholar	rs757905943
google	rs757905943
pharmgkb	rs757905943
gwascentral	rs757905943
openSNP	rs757905943
23andMe	rs757905943
SNPshot	rs757905943
SNPdbe	rs757905943
MSV3d	rs757905943
GWAS Ctlg	rs757905943

Max Magnitude

0

ClinVar
Risk	rs757905943(A;A)
Alt	rs757905943(A;A)
Reference	Rs757905943(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ACSF3
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.89167437G>A
CLNSRC
CLNACC	RCV000185754.1,