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rs776140816

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776140816(C;C)
Make rs776140816(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position40017243
GeneEIF2AK4
is asnp
is mentioned by
dbSNPrs776140816
dbSNP (classic)rs776140816
ClinGenrs776140816
ebirs776140816
HLIrs776140816
Exacrs776140816
Gnomadrs776140816
Varsomers776140816
LitVarrs776140816
Maprs776140816
PheGenIrs776140816
Biobankrs776140816
1000 genomesrs776140816
hgdprs776140816
ensemblrs776140816
geneviewrs776140816
scholarrs776140816
googlers776140816
pharmgkbrs776140816
gwascentralrs776140816
openSNPrs776140816
23andMers776140816
SNPshotrs776140816
SNPdbers776140816
MSV3drs776140816
GWAS Ctlgrs776140816
Max Magnitude0
ClinVar
Risk rs776140816(A;A) rs776140816(C;C)
Alt rs776140816(A;A) rs776140816(C;C)
Reference Rs776140816(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.40309444G>C
CLNSRC
CLNACC RCV000488628.1,