rs202247795

Orientation

plus

Stabilized

plus

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

Make rs202247795(C;T)

Make rs202247795(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

211702102

Gene

ERBB4

is a	snp
is	mentioned by
dbSNP	rs202247795
dbSNP (classic)	rs202247795
ClinGen	rs202247795
ebi	rs202247795
HLI	rs202247795
Exac	rs202247795
Gnomad	rs202247795
Varsome	rs202247795
LitVar	rs202247795
Map	rs202247795
PheGenI	rs202247795
Biobank	rs202247795
1000 genomes	rs202247795
hgdp	rs202247795
ensembl	rs202247795
geneview	rs202247795
scholar	rs202247795
google	rs202247795
pharmgkb	rs202247795
gwascentral	rs202247795
openSNP	rs202247795
23andMe	rs202247795
SNPshot	rs202247795
SNPdbe	rs202247795
MSV3d	rs202247795
GWAS Ctlg	rs202247795

Max Magnitude

0

ClinVar
Risk	rs202247795(T;T)
Alt	rs202247795(T;T)
Reference	Rs202247795(C;C)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	ERBB4
CLNDBN	Malignant melanoma
Reversed	0
HGVS	NC_000002.11:g.212566827C>T
CLNSRC
CLNACC	RCV000443453.1,