rs55671017

Orientation

plus

Stabilized

plus

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

Make rs55671017(G;T)

Make rs55671017(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

211705339

Gene

ERBB4

is a	snp
is	mentioned by
dbSNP	rs55671017
dbSNP (classic)	rs55671017
ClinGen	rs55671017
ebi	rs55671017
HLI	rs55671017
Exac	rs55671017
Gnomad	rs55671017
Varsome	rs55671017
LitVar	rs55671017
Map	rs55671017
PheGenI	rs55671017
Biobank	rs55671017
1000 genomes	rs55671017
hgdp	rs55671017
ensembl	rs55671017
geneview	rs55671017
scholar	rs55671017
google	rs55671017
pharmgkb	rs55671017
gwascentral	rs55671017
openSNP	rs55671017
23andMe	rs55671017
SNPshot	rs55671017
SNPdbe	rs55671017
MSV3d	rs55671017
GWAS Ctlg	rs55671017

Max Magnitude

0

ClinVar
Risk	rs55671017(A;A) rs55671017(T;T)
Alt	rs55671017(A;A) rs55671017(T;T)
Reference	Rs55671017(G;G)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	ERBB4
CLNDBN	Malignant melanoma
Reversed	0
HGVS	NC_000002.11:g.212570064G>A
CLNSRC
CLNACC	RCV000424857.1,