rs558274487

Orientation

plus

Stabilized

plus

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

Make rs558274487(A;A)

Make rs558274487(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

127939952

Gene

MFSD8

is a	snp
is	mentioned by
dbSNP	rs558274487
dbSNP (classic)	rs558274487
ClinGen	rs558274487
ebi	rs558274487
HLI	rs558274487
Exac	rs558274487
Gnomad	rs558274487
Varsome	rs558274487
LitVar	rs558274487
Map	rs558274487
PheGenI	rs558274487
Biobank	rs558274487
1000 genomes	rs558274487
hgdp	rs558274487
ensembl	rs558274487
geneview	rs558274487
scholar	rs558274487
google	rs558274487
pharmgkb	rs558274487
gwascentral	rs558274487
openSNP	rs558274487
23andMe	rs558274487
SNPshot	rs558274487
SNPdbe	rs558274487
MSV3d	rs558274487
GWAS Ctlg	rs558274487

Max Magnitude

0

ClinVar
Risk	rs558274487(A;A) rs558274487(T;T)
Alt	rs558274487(A;A) rs558274487(T;T)
Reference	Rs558274487(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MFSD8
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.128861107C>T
CLNSRC
CLNACC	RCV000188167.1,