rs202182978

Orientation

plus

Stabilized

plus

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

Make rs202182978(C;T)

Make rs202182978(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

89100709

Gene

ACSF3

is a	snp
is	mentioned by
dbSNP	rs202182978
dbSNP (classic)	rs202182978
ClinGen	rs202182978
ebi	rs202182978
HLI	rs202182978
Exac	rs202182978
Gnomad	rs202182978
Varsome	rs202182978
LitVar	rs202182978
Map	rs202182978
PheGenI	rs202182978
Biobank	rs202182978
1000 genomes	rs202182978
hgdp	rs202182978
ensembl	rs202182978
geneview	rs202182978
scholar	rs202182978
google	rs202182978
pharmgkb	rs202182978
gwascentral	rs202182978
openSNP	rs202182978
23andMe	rs202182978
SNPshot	rs202182978
SNPdbe	rs202182978
MSV3d	rs202182978
GWAS Ctlg	rs202182978

Max Magnitude

0

ClinVar
Risk	rs202182978(A;A) rs202182978(T;T)
Alt	rs202182978(A;A) rs202182978(T;T)
Reference	Rs202182978(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ACSF3
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.89167117C>T
CLNSRC
CLNACC	RCV000224144.1,