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rs28931572

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0
(T;T) 0 common in complete genomics
Make rs28931572(A;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position94382891
GeneSERPINA1
is asnp
is mentioned by
dbSNPrs28931572
ebirs28931572
HLIrs28931572
Exacrs28931572
Varsomers28931572
Maprs28931572
PheGenIrs28931572
hapmaprs28931572
1000 genomesrs28931572
hgdprs28931572
ensemblrs28931572
gopubmedrs28931572
geneviewrs28931572
scholarrs28931572
googlers28931572
pharmgkbrs28931572
gwascentralrs28931572
openSNPrs28931572
23andMers28931572
23andMe allrs28931572
SNP Nexus

SNPshotrs28931572
SNPdbers28931572
MSV3drs28931572
GWAS Ctlgrs28931572
Max Magnitude0
OMIM107400
DescPI NULL(LUDWIGSHAFEN)
Variant0031
Relatedalso
Neighborrs709932
Distance27
Neighborrs28931568
Distance75


ClinVar
Risk rs28931572(A;A)
Alt rs28931572(A;A)
Reference rs28931572(T;T)
Significance Other
Disease PI NULL(LUDWIGSHAFEN) PI Q0(LUDWIGSHAFEN) Alpha-1-antitrypsin deficiency
Variation info
Gene SERPINA1
CLNDBN PI NULL(LUDWIGSHAFEN) PI Q0(LUDWIGSHAFEN) Alpha-1-antitrypsin deficiency
Reversed 1
HGVS NC_000014.8:g.94849228A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019601.3, RCV000019602.3, RCV000201851.1,



[PMID 18974877OA-icon.png] Modifier effects between regulatory and protein-coding variation.