rs761645282

Orientation

plus

Stabilized

plus

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

Make rs761645282(C;C)

Make rs761645282(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

74718992

Gene

FA2H

is a	snp
is	mentioned by
dbSNP	rs761645282
dbSNP (classic)	rs761645282
ClinGen	rs761645282
ebi	rs761645282
HLI	rs761645282
Exac	rs761645282
Gnomad	rs761645282
Varsome	rs761645282
LitVar	rs761645282
Map	rs761645282
PheGenI	rs761645282
Biobank	rs761645282
1000 genomes	rs761645282
hgdp	rs761645282
ensembl	rs761645282
geneview	rs761645282
scholar	rs761645282
google	rs761645282
pharmgkb	rs761645282
gwascentral	rs761645282
openSNP	rs761645282
23andMe	rs761645282
SNPshot	rs761645282
SNPdbe	rs761645282
MSV3d	rs761645282
GWAS Ctlg	rs761645282

Max Magnitude

0

ClinVar
Risk	rs761645282(C;C)
Alt	rs761645282(C;C)
Reference	Rs761645282(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FA2H
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.74752890T>C
CLNSRC
CLNACC	RCV000414400.1,