rs104893856

Orientation

minus

Stabilized

minus

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

Make rs104893856(A;A)

Make rs104893856(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

41746162

Gene

PHOX2B

is a	snp
is	mentioned by
dbSNP	rs104893856
dbSNP (classic)	rs104893856
ClinGen	rs104893856
ebi	rs104893856
HLI	rs104893856
Exac	rs104893856
Gnomad	rs104893856
Varsome	rs104893856
LitVar	rs104893856
Map	rs104893856
PheGenI	rs104893856
Biobank	rs104893856
1000 genomes	rs104893856
hgdp	rs104893856
ensembl	rs104893856
geneview	rs104893856
scholar	rs104893856
google	rs104893856
pharmgkb	rs104893856
gwascentral	rs104893856
openSNP	rs104893856
23andMe	rs104893856
SNPshot	rs104893856
SNPdbe	rs104893856
MSV3d	rs104893856
GWAS Ctlg	rs104893856

Max Magnitude

0

OMIM	603851
Desc
Variant	0008
Related	also

ClinVar
Risk	rs104893856(A;A)
Alt	rs104893856(A;A)
Reference	Rs104893856(G;G)
Significance	Other
Disease	Neuroblastoma 2
Variation	info
Gene	PHOX2B
CLNDBN	Neuroblastoma 2
Reversed	1
HGVS	NC_000004.11:g.41748179C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006385.2,