Have questions? Visit https://www.reddit.com/r/SNPedia

rs535202189

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs535202189(C;T)
Make rs535202189(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position211673256
GeneERBB4
is asnp
is mentioned by
dbSNPrs535202189
dbSNP (old)rs535202189
ClinGenrs535202189
ebirs535202189
HLIrs535202189
Exacrs535202189
Gnomadrs535202189
Varsomers535202189
Maprs535202189
PheGenIrs535202189
Biobankrs535202189
1000 genomesrs535202189
hgdprs535202189
ensemblrs535202189
gopubmedrs535202189
geneviewrs535202189
scholarrs535202189
googlers535202189
pharmgkbrs535202189
gwascentralrs535202189
openSNPrs535202189
23andMers535202189
23andMe allrs535202189
SNP Nexus

SNPshotrs535202189
SNPdbers535202189
MSV3drs535202189
GWAS Ctlgrs535202189
Max Magnitude0
ClinVar
Risk rs535202189(T;T)
Alt rs535202189(T;T)
Reference Rs535202189(C;C)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene ERBB4
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000002.11:g.212537981C>T
CLNSRC
CLNACC RCV000431732.1,