rs765086319

Orientation

plus

Stabilized

plus

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

Make rs765086319(A;A)

Make rs765086319(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

74726273

Gene

FA2H

is a	snp
is	mentioned by
dbSNP	rs765086319
dbSNP (classic)	rs765086319
ClinGen	rs765086319
ebi	rs765086319
HLI	rs765086319
Exac	rs765086319
Gnomad	rs765086319
Varsome	rs765086319
LitVar	rs765086319
Map	rs765086319
PheGenI	rs765086319
Biobank	rs765086319
1000 genomes	rs765086319
hgdp	rs765086319
ensembl	rs765086319
geneview	rs765086319
scholar	rs765086319
google	rs765086319
pharmgkb	rs765086319
gwascentral	rs765086319
openSNP	rs765086319
23andMe	rs765086319
SNPshot	rs765086319
SNPdbe	rs765086319
MSV3d	rs765086319
GWAS Ctlg	rs765086319

Max Magnitude

0

ClinVar
Risk	rs765086319(A;A)
Alt	rs765086319(A;A)
Reference	Rs765086319(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	FA2H
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000016.9:g.74760171G>A
CLNSRC
CLNACC	RCV000190745.1,