rs113994115

Orientation

plus

Stabilized

plus

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

Make rs113994115(G;T)

Make rs113994115(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

15942281

Gene	MYCN, MYCNOS

is a	snp
is	mentioned by
dbSNP	rs113994115
dbSNP (classic)	rs113994115
ClinGen	rs113994115
ebi	rs113994115
HLI	rs113994115
Exac	rs113994115
Gnomad	rs113994115
Varsome	rs113994115
LitVar	rs113994115
Map	rs113994115
PheGenI	rs113994115
Biobank	rs113994115
1000 genomes	rs113994115
hgdp	rs113994115
ensembl	rs113994115
geneview	rs113994115
scholar	rs113994115
google	rs113994115
pharmgkb	rs113994115
gwascentral	rs113994115
openSNP	rs113994115
23andMe	rs113994115
SNPshot	rs113994115
SNPdbe	rs113994115
MSV3d	rs113994115
GWAS Ctlg	rs113994115

Max Magnitude

0

OMIM	164840
Desc
Variant	0004
Related	also

ClinVar
Risk	rs113994115(T;T)
Alt	rs113994115(T;T)
Reference	Rs113994115(G;G)
Significance	Pathogenic
Disease	Feingold syndrome 1
Variation	info
Gene	MYCN MYCNOS
CLNDBN	Feingold syndrome 1
Reversed	0
HGVS	NC_000002.11:g.16082403G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014910.25,