rs796052752

Orientation

minus

Stabilized

minus

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

Make rs796052752(-;A)

Make rs796052752(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

127943973

Gene

MFSD8

is a	snp
is	mentioned by
dbSNP	rs796052752
dbSNP (classic)	rs796052752
ClinGen	rs796052752
ebi	rs796052752
HLI	rs796052752
Exac	rs796052752
Gnomad	rs796052752
Varsome	rs796052752
LitVar	rs796052752
Map	rs796052752
PheGenI	rs796052752
Biobank	rs796052752
1000 genomes	rs796052752
hgdp	rs796052752
ensembl	rs796052752
geneview	rs796052752
scholar	rs796052752
google	rs796052752
pharmgkb	rs796052752
gwascentral	rs796052752
openSNP	rs796052752
23andMe	rs796052752
SNPshot	rs796052752
SNPdbe	rs796052752
MSV3d	rs796052752
GWAS Ctlg	rs796052752

Max Magnitude

0

ClinVar
Risk	rs796052752(A;A)
Alt	rs796052752(A;A)
Reference	Rs796052752(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MFSD8
CLNDBN	not provided
Reversed	1
HGVS	NC_000004.11:g.128865129dupT
CLNSRC
CLNACC	RCV000188195.1,