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rs1028250483

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1028250483(C;T)
Make rs1028250483(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position156175179
GeneSEMA4A
is asnp
is mentioned by
dbSNPrs1028250483
dbSNP (old)rs1028250483
ClinGenrs1028250483
ebirs1028250483
HLIrs1028250483
Exacrs1028250483
Gnomadrs1028250483
Varsomers1028250483
LitVarrs1028250483
Maprs1028250483
PheGenIrs1028250483
Biobankrs1028250483
1000 genomesrs1028250483
hgdprs1028250483
ensemblrs1028250483
gopubmedrs1028250483
geneviewrs1028250483
scholarrs1028250483
googlers1028250483
pharmgkbrs1028250483
gwascentralrs1028250483
openSNPrs1028250483
23andMers1028250483
23andMe allrs1028250483
SNPshotrs1028250483
SNPdbers1028250483
MSV3drs1028250483
GWAS Ctlgrs1028250483
Max Magnitude0
ClinVar
Risk rs1028250483(T;T)
Alt rs1028250483(T;T)
Reference Rs1028250483(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SEMA4A
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156144970C>T
CLNSRC
CLNACC RCV000437436.1,