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rs148188503

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs148188503(C;T)
Make rs148188503(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position55181364
GeneEGFR, EGFR-AS1
is asnp
is mentioned by
dbSNPrs148188503
dbSNP (old)rs148188503
ClinGenrs148188503
ebirs148188503
HLIrs148188503
Exacrs148188503
Gnomadrs148188503
Varsomers148188503
Maprs148188503
PheGenIrs148188503
Biobankrs148188503
1000 genomesrs148188503
hgdprs148188503
ensemblrs148188503
gopubmedrs148188503
geneviewrs148188503
scholarrs148188503
googlers148188503
pharmgkbrs148188503
gwascentralrs148188503
openSNPrs148188503
23andMers148188503
23andMe allrs148188503
SNPshotrs148188503
SNPdbers148188503
MSV3drs148188503
GWAS Ctlgrs148188503
Max Magnitude0

[PMID 27895798OA-icon.png] Exploring the impact of EGFR T790M neighboring SNPs on ARMS-based T790M mutation assay.

ClinVar
Risk rs148188503(T;T)
Alt rs148188503(T;T)
Reference Rs148188503(C;C)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene EGFR EGFR-AS1
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.55249057C>T
CLNSRC
CLNACC RCV000038426.2,