rs104893855

Orientation

minus

Stabilized

minus

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

Make rs104893855(G;T)

Make rs104893855(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

41747479

Gene	LOC105374425, PHOX2B

is a	snp
is	mentioned by
dbSNP	rs104893855
dbSNP (classic)	rs104893855
ClinGen	rs104893855
ebi	rs104893855
HLI	rs104893855
Exac	rs104893855
Gnomad	rs104893855
Varsome	rs104893855
LitVar	rs104893855
Map	rs104893855
PheGenI	rs104893855
Biobank	rs104893855
1000 genomes	rs104893855
hgdp	rs104893855
ensembl	rs104893855
geneview	rs104893855
scholar	rs104893855
google	rs104893855
pharmgkb	rs104893855
gwascentral	rs104893855
openSNP	rs104893855
23andMe	rs104893855
SNPshot	rs104893855
SNPdbe	rs104893855
MSV3d	rs104893855
GWAS Ctlg	rs104893855

Max Magnitude

0

OMIM	603851
Desc
Variant	0005
Related	also

ClinVar
Risk	rs104893855(T;T)
Alt	rs104893855(T;T)
Reference	Rs104893855(G;G)
Significance	Other
Disease	Neuroblastoma 2
Variation	info
Gene	PHOX2B
CLNDBN	Neuroblastoma 2
Reversed	1
HGVS	NC_000004.11:g.41749496C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006382.3,