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rs886037661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886037661(A;A)
Make rs886037661(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome15
Position39965685
GeneEIF2AK4
is asnp
is mentioned by
dbSNPrs886037661
dbSNP (classic)rs886037661
ClinGenrs886037661
ebirs886037661
HLIrs886037661
Exacrs886037661
Gnomadrs886037661
Varsomers886037661
LitVarrs886037661
Maprs886037661
PheGenIrs886037661
Biobankrs886037661
1000 genomesrs886037661
hgdprs886037661
ensemblrs886037661
geneviewrs886037661
scholarrs886037661
googlers886037661
pharmgkbrs886037661
gwascentralrs886037661
openSNPrs886037661
23andMers886037661
SNPshotrs886037661
SNPdbers886037661
MSV3drs886037661
GWAS Ctlgrs886037661
Max Magnitude0
ClinVar
Risk rs886037661(A;A)
Alt rs886037661(A;A)
Reference Rs886037661(G;G)
Significance Pathogenic
Disease Familial pulmonary capillary hemangiomatosis
Variation info
Gene EIF2AK4
CLNDBN Familial pulmonary capillary hemangiomatosis
Reversed 0
HGVS NC_000015.9:g.40257886G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000087758.6,