rs751010275

Orientation

plus

Stabilized

plus

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

Make rs751010275(A;C)

Make rs751010275(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

127938843

Gene

MFSD8

is a	snp
is	mentioned by
dbSNP	rs751010275
dbSNP (classic)	rs751010275
ClinGen	rs751010275
ebi	rs751010275
HLI	rs751010275
Exac	rs751010275
Gnomad	rs751010275
Varsome	rs751010275
LitVar	rs751010275
Map	rs751010275
PheGenI	rs751010275
Biobank	rs751010275
1000 genomes	rs751010275
hgdp	rs751010275
ensembl	rs751010275
geneview	rs751010275
scholar	rs751010275
google	rs751010275
pharmgkb	rs751010275
gwascentral	rs751010275
openSNP	rs751010275
23andMe	rs751010275
SNPshot	rs751010275
SNPdbe	rs751010275
MSV3d	rs751010275
GWAS Ctlg	rs751010275

Max Magnitude

0

ClinVar
Risk	rs751010275(C;C)
Alt	rs751010275(C;C)
Reference	Rs751010275(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MFSD8
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.128859998A>C
CLNSRC
CLNACC	RCV000188190.1,