rs1057518032

Orientation

minus

Stabilized

minus

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

Make rs1057518032(A;A)

Make rs1057518032(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

74774617

Gene

FA2H

is a	snp
is	mentioned by
dbSNP	rs1057518032
dbSNP (classic)	rs1057518032
ClinGen	rs1057518032
ebi	rs1057518032
HLI	rs1057518032
Exac	rs1057518032
Gnomad	rs1057518032
Varsome	rs1057518032
LitVar	rs1057518032
Map	rs1057518032
PheGenI	rs1057518032
Biobank	rs1057518032
1000 genomes	rs1057518032
hgdp	rs1057518032
ensembl	rs1057518032
geneview	rs1057518032
scholar	rs1057518032
google	rs1057518032
pharmgkb	rs1057518032
gwascentral	rs1057518032
openSNP	rs1057518032
23andMe	rs1057518032
SNPshot	rs1057518032
SNPdbe	rs1057518032
MSV3d	rs1057518032
GWAS Ctlg	rs1057518032

Max Magnitude

0

ClinVar
Risk	rs1057518032(A;A)
Alt	rs1057518032(A;A)
Reference	Rs1057518032(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FA2H
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.74808515C>T
CLNSRC
CLNACC	RCV000413571.1,