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rs267599192

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267599192(A;A)
Make rs267599192(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position211673250
GeneERBB4
is asnp
is mentioned by
dbSNPrs267599192
dbSNP (old)rs267599192
ClinGenrs267599192
ebirs267599192
HLIrs267599192
Exacrs267599192
Gnomadrs267599192
Varsomers267599192
Maprs267599192
PheGenIrs267599192
Biobankrs267599192
1000 genomesrs267599192
hgdprs267599192
ensemblrs267599192
gopubmedrs267599192
geneviewrs267599192
scholarrs267599192
googlers267599192
pharmgkbrs267599192
gwascentralrs267599192
openSNPrs267599192
23andMers267599192
23andMe allrs267599192
SNP Nexus

SNPshotrs267599192
SNPdbers267599192
MSV3drs267599192
GWAS Ctlgrs267599192
Max Magnitude0
ClinVar
Risk rs267599192(A;A)
Alt rs267599192(A;A)
Reference Rs267599192(G;G)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene ERBB4
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000002.11:g.212537975G>A
CLNSRC
CLNACC RCV000422332.1,