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rs146387238

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146387238(A;A)
Make rs146387238(A;C)
ReferenceGRCh38 38.1/142
Chromosome4
Position154587511
GeneFGA
is asnp
is mentioned by
dbSNPrs146387238
ebirs146387238
HLIrs146387238
Exacrs146387238
Varsomers146387238
Maprs146387238
PheGenIrs146387238
hapmaprs146387238
1000 genomesrs146387238
hgdprs146387238
ensemblrs146387238
gopubmedrs146387238
geneviewrs146387238
scholarrs146387238
googlers146387238
pharmgkbrs146387238
gwascentralrs146387238
openSNPrs146387238
23andMers146387238
23andMe allrs146387238
SNP Nexus

SNPshotrs146387238
SNPdbers146387238
MSV3drs146387238
GWAS Ctlgrs146387238
Max Magnitude0
ClinVar
Risk rs146387238(A,G;A,G)
Alt rs146387238(A,G;A,G)
Reference rs146387238(C;C)
Significance Pathogenic
Disease Afibrinogenemia Hypodysfibrinogenemia
Variation info
Gene FGA
CLNDBN Afibrinogenemia, congenital Hypodysfibrinogenemia, congenital
Reversed 0
HGVS NC_000004.11:g.155508663C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017877.27, RCV000030942.27,