rs6871748

Orientation

plus

Stabilized

plus

Make rs6871748(C;C)

Make rs6871748(C;T)

Make rs6871748(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

35885880

is a	snp
is	mentioned by
dbSNP	rs6871748
dbSNP (classic)	rs6871748
ClinGen	rs6871748
ebi	rs6871748
HLI	rs6871748
Exac	rs6871748
Gnomad	rs6871748
Varsome	rs6871748
LitVar	rs6871748
Map	rs6871748
PheGenI	rs6871748
Biobank	rs6871748
1000 genomes	rs6871748
hgdp	rs6871748
ensembl	rs6871748
geneview	rs6871748
scholar	rs6871748
google	rs6871748
pharmgkb	rs6871748
gwascentral	rs6871748
openSNP	rs6871748
23andMe	rs6871748
SNPshot	rs6871748
SNPdbe	rs6871748
MSV3d	rs6871748
GWAS Ctlg	rs6871748

GMAF

0.1938

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

OMIM	612595
Desc	MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 3; MS3
Variant
Related	also

[PMID 19221116] Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.