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rs606231253

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231253(A;A)
Make rs606231253(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position55157738
GeneEGFR
is asnp
is mentioned by
dbSNPrs606231253
ebirs606231253
HLIrs606231253
Exacrs606231253
Varsomers606231253
Maprs606231253
PheGenIrs606231253
hapmaprs606231253
1000 genomesrs606231253
hgdprs606231253
ensemblrs606231253
gopubmedrs606231253
geneviewrs606231253
scholarrs606231253
googlers606231253
pharmgkbrs606231253
gwascentralrs606231253
openSNPrs606231253
23andMers606231253
23andMe allrs606231253
SNP Nexus

SNPshotrs606231253
SNPdbers606231253
MSV3drs606231253
GWAS Ctlgrs606231253
Max Magnitude0
ClinVar
Risk rs606231253(A;A)
Alt rs606231253(A;A)
Reference rs606231253(G;G)
Significance Pathogenic
Disease Inflammatory skin and bowel disease
Variation info
Gene EGFR
CLNDBN Inflammatory skin and bowel disease, neonatal, 2
Reversed 0
HGVS NC_000007.13:g.55225431G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144851.5,