rs121913666

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs121913666(A;A)

Make rs121913666(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

15945847

Gene

MYCN

is a	snp
is	mentioned by
dbSNP	rs121913666
dbSNP (classic)	rs121913666
ClinGen	rs121913666
ebi	rs121913666
HLI	rs121913666
Exac	rs121913666
Gnomad	rs121913666
Varsome	rs121913666
LitVar	rs121913666
Map	rs121913666
PheGenI	rs121913666
Biobank	rs121913666
1000 genomes	rs121913666
hgdp	rs121913666
ensembl	rs121913666
geneview	rs121913666
scholar	rs121913666
google	rs121913666
pharmgkb	rs121913666
gwascentral	rs121913666
openSNP	rs121913666
23andMe	rs121913666
SNPshot	rs121913666
SNPdbe	rs121913666
MSV3d	rs121913666
GWAS Ctlg	rs121913666

Max Magnitude

0

OMIM	164840
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121913666(A;A)
Alt	rs121913666(A;A)
Reference	Rs121913666(G;G)
Significance	Pathogenic
Disease	Feingold syndrome 1
Variation	info
Gene	MYCN
CLNDBN	Feingold syndrome 1
Reversed	0
HGVS	NC_000002.11:g.16085969G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014912.21,