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rs886037891

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886037891(G;T)
Make rs886037891(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome7
Position55155917
GeneEGFR
is asnp
is mentioned by
dbSNPrs886037891
dbSNP (classic)rs886037891
ClinGenrs886037891
ebirs886037891
HLIrs886037891
Exacrs886037891
Gnomadrs886037891
Varsomers886037891
LitVarrs886037891
Maprs886037891
PheGenIrs886037891
Biobankrs886037891
1000 genomesrs886037891
hgdprs886037891
ensemblrs886037891
geneviewrs886037891
scholarrs886037891
googlers886037891
pharmgkbrs886037891
gwascentralrs886037891
openSNPrs886037891
23andMers886037891
23andMe allrs886037891
SNPshotrs886037891
SNPdbers886037891
MSV3drs886037891
GWAS Ctlgrs886037891
Max Magnitude0
ClinVar
Risk rs886037891(T;T)
Alt rs886037891(T;T)
Reference Rs886037891(G;G)
Significance Pathogenic
Disease Cowden syndrome 1
Variation info
Gene EGFR
CLNDBN Cowden syndrome 1
Reversed 0
HGVS NC_000007.13:g.55223610G>T
CLNSRC
CLNACC RCV000256393.1,