rs121434504

Orientation

plus

Stabilized

plus

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

Make rs121434504(A;G)

Make rs121434504(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

108753474

Gene

RANBP2

is a	snp
is	mentioned by
dbSNP	rs121434504
dbSNP (classic)	rs121434504
ClinGen	rs121434504
ebi	rs121434504
HLI	rs121434504
Exac	rs121434504
Gnomad	rs121434504
Varsome	rs121434504
LitVar	rs121434504
Map	rs121434504
PheGenI	rs121434504
Biobank	rs121434504
1000 genomes	rs121434504
hgdp	rs121434504
ensembl	rs121434504
geneview	rs121434504
scholar	rs121434504
google	rs121434504
pharmgkb	rs121434504
gwascentral	rs121434504
openSNP	rs121434504
23andMe	rs121434504
SNPshot	rs121434504
SNPdbe	rs121434504
MSV3d	rs121434504
GWAS Ctlg	rs121434504

Max Magnitude

0

OMIM	601181
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121434504(G;G)
Alt	rs121434504(G;G)
Reference	Rs121434504(A;A)
Significance	Other
Disease	Encephalopathy
Variation	info
Gene	RANBP2
CLNDBN	Encephalopathy, acute, infection-induced, 3, suceptibility to
Reversed	0
HGVS	NC_000002.11:g.109369930A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008870.2,