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rs4371677

From SNPedia

Orientationplus
Stabilizedplus
Make rs4371677(A;A)
Make rs4371677(A;G)
Make rs4371677(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position56650730
GeneHOPX
is asnp
is mentioned by
dbSNPrs4371677
ebirs4371677
HLIrs4371677
Exacrs4371677
Varsomers4371677
Maprs4371677
PheGenIrs4371677
hapmaprs4371677
1000 genomesrs4371677
hgdprs4371677
ensemblrs4371677
gopubmedrs4371677
geneviewrs4371677
scholarrs4371677
googlers4371677
pharmgkbrs4371677
gwascentralrs4371677
openSNPrs4371677
23andMers4371677
23andMe allrs4371677
SNP Nexus

SNPshotrs4371677
SNPdbers4371677
MSV3drs4371677
GWAS Ctlgrs4371677
GMAF0.4931
Max Magnitude
? (A;A) (A;G) (G;G) 28


Venter snp
Source plos
Gene HOP_HUMAN
allele A
frequency 0.442
sift
HuRef 1103654417252
Disease Association Defects in HOP may be a cause of various types of cancer, such as lung cancer, choriocarcinoma, head and neck squamous cell carcinoma and oral squamous cell carcinoma.



GET Evidence
HOPX-P94L
aa_change Pro94Leu
aa_change_short P94L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency
summary