rs1057521784

Orientation

plus

Stabilized

plus

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

Make rs1057521784(A;A)

Make rs1057521784(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

100105985

Gene

AP4M1

is a	snp
is	mentioned by
dbSNP	rs1057521784
dbSNP (classic)	rs1057521784
ClinGen	rs1057521784
ebi	rs1057521784
HLI	rs1057521784
Exac	rs1057521784
Gnomad	rs1057521784
Varsome	rs1057521784
LitVar	rs1057521784
Map	rs1057521784
PheGenI	rs1057521784
Biobank	rs1057521784
1000 genomes	rs1057521784
hgdp	rs1057521784
ensembl	rs1057521784
geneview	rs1057521784
scholar	rs1057521784
google	rs1057521784
pharmgkb	rs1057521784
gwascentral	rs1057521784
openSNP	rs1057521784
23andMe	rs1057521784
SNPshot	rs1057521784
SNPdbe	rs1057521784
MSV3d	rs1057521784
GWAS Ctlg	rs1057521784

Max Magnitude

0

ClinVar
Risk	rs1057521784(A;A)
Alt	rs1057521784(A;A)
Reference	Rs1057521784(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	AP4M1
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.99703608G>A
CLNSRC
CLNACC	RCV000422720.1,