rs796052747

Orientation

minus

Stabilized

minus

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

Make rs796052747(A;A)

Make rs796052747(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

127920749

Gene

MFSD8

is a	snp
is	mentioned by
dbSNP	rs796052747
dbSNP (classic)	rs796052747
ClinGen	rs796052747
ebi	rs796052747
HLI	rs796052747
Exac	rs796052747
Gnomad	rs796052747
Varsome	rs796052747
LitVar	rs796052747
Map	rs796052747
PheGenI	rs796052747
Biobank	rs796052747
1000 genomes	rs796052747
hgdp	rs796052747
ensembl	rs796052747
geneview	rs796052747
scholar	rs796052747
google	rs796052747
pharmgkb	rs796052747
gwascentral	rs796052747
openSNP	rs796052747
23andMe	rs796052747
SNPshot	rs796052747
SNPdbe	rs796052747
MSV3d	rs796052747
GWAS Ctlg	rs796052747

Max Magnitude

0

ClinVar
Risk	rs796052747(A;A)
Alt	rs796052747(A;A)
Reference	Rs796052747(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MFSD8
CLNDBN	not provided
Reversed	1
HGVS	NC_000004.11:g.128841904C>T
CLNSRC
CLNACC	RCV000188185.1,