rs796052742

Orientation

minus

Stabilized

minus

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

Make rs796052742(A;G)

Make rs796052742(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

127942156

Gene

MFSD8

is a	snp
is	mentioned by
dbSNP	rs796052742
dbSNP (classic)	rs796052742
ClinGen	rs796052742
ebi	rs796052742
HLI	rs796052742
Exac	rs796052742
Gnomad	rs796052742
Varsome	rs796052742
LitVar	rs796052742
Map	rs796052742
PheGenI	rs796052742
Biobank	rs796052742
1000 genomes	rs796052742
hgdp	rs796052742
ensembl	rs796052742
geneview	rs796052742
scholar	rs796052742
google	rs796052742
pharmgkb	rs796052742
gwascentral	rs796052742
openSNP	rs796052742
23andMe	rs796052742
SNPshot	rs796052742
SNPdbe	rs796052742
MSV3d	rs796052742
GWAS Ctlg	rs796052742

Max Magnitude

0

ClinVar
Risk	rs796052742(G;G)
Alt	rs796052742(G;G)
Reference	Rs796052742(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MFSD8
CLNDBN	not provided
Reversed	1
HGVS	NC_000004.11:g.128863311T>C
CLNSRC
CLNACC	RCV000188168.1,