rs121434502

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs121434502(C;T)

Make rs121434502(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

108751993

Gene

RANBP2

is a	snp
is	mentioned by
dbSNP	rs121434502
dbSNP (classic)	rs121434502
ClinGen	rs121434502
ebi	rs121434502
HLI	rs121434502
Exac	rs121434502
Gnomad	rs121434502
Varsome	rs121434502
LitVar	rs121434502
Map	rs121434502
PheGenI	rs121434502
Biobank	rs121434502
1000 genomes	rs121434502
hgdp	rs121434502
ensembl	rs121434502
geneview	rs121434502
scholar	rs121434502
google	rs121434502
pharmgkb	rs121434502
gwascentral	rs121434502
openSNP	rs121434502
23andMe	rs121434502
SNPshot	rs121434502
SNPdbe	rs121434502
MSV3d	rs121434502
GWAS Ctlg	rs121434502

Max Magnitude

0

OMIM	601181
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121434502(T;T)
Alt	rs121434502(T;T)
Reference	Rs121434502(C;C)
Significance	Other
Disease	Encephalopathy
Variation	info
Gene	RANBP2
CLNDBN	Encephalopathy, acute, infection-induced, 3, suceptibility to
Reversed	0
HGVS	NC_000002.11:g.109368449C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008868.2,