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

rs202247795

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs202247795(C;T)
Make rs202247795(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position211702102
GeneERBB4
is asnp
is mentioned by
dbSNPrs202247795
dbSNP (old)rs202247795
ClinGenrs202247795
ebirs202247795
HLIrs202247795
Exacrs202247795
Gnomadrs202247795
Varsomers202247795
Maprs202247795
PheGenIrs202247795
Biobankrs202247795
1000 genomesrs202247795
hgdprs202247795
ensemblrs202247795
gopubmedrs202247795
geneviewrs202247795
scholarrs202247795
googlers202247795
pharmgkbrs202247795
gwascentralrs202247795
openSNPrs202247795
23andMers202247795
23andMe allrs202247795
SNP Nexus

SNPshotrs202247795
SNPdbers202247795
MSV3drs202247795
GWAS Ctlgrs202247795
Max Magnitude0
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,