rs766140986

Orientation

plus

Stabilized

plus

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

Make rs766140986(C;T)

Make rs766140986(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

75761228

Gene

ACADM

is a	snp
is	mentioned by
dbSNP	rs766140986
dbSNP (classic)	rs766140986
ClinGen	rs766140986
ebi	rs766140986
HLI	rs766140986
Exac	rs766140986
Gnomad	rs766140986
Varsome	rs766140986
LitVar	rs766140986
Map	rs766140986
PheGenI	rs766140986
Biobank	rs766140986
1000 genomes	rs766140986
hgdp	rs766140986
ensembl	rs766140986
geneview	rs766140986
scholar	rs766140986
google	rs766140986
pharmgkb	rs766140986
gwascentral	rs766140986
openSNP	rs766140986
23andMe	rs766140986
SNPshot	rs766140986
SNPdbe	rs766140986
MSV3d	rs766140986
GWAS Ctlg	rs766140986

Max Magnitude

0

ClinVar
Risk	rs766140986(T;T)
Alt	rs766140986(T;T)
Reference	Rs766140986(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ACADM
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.76226913C>T
CLNSRC
CLNACC	RCV000185667.3,