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rs773004449

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773004449(C;T)
Make rs773004449(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position55694522
GeneITGA7
is asnp
is mentioned by
dbSNPrs773004449
ebirs773004449
HLIrs773004449
Exacrs773004449
Varsomers773004449
Maprs773004449
PheGenIrs773004449
hapmaprs773004449
1000 genomesrs773004449
hgdprs773004449
ensemblrs773004449
gopubmedrs773004449
geneviewrs773004449
scholarrs773004449
googlers773004449
pharmgkbrs773004449
gwascentralrs773004449
openSNPrs773004449
23andMers773004449
23andMe allrs773004449
SNP Nexus

SNPshotrs773004449
SNPdbers773004449
MSV3drs773004449
GWAS Ctlgrs773004449
Max Magnitude0
ClinVar
Risk rs773004449(T;T)
Alt rs773004449(T;T)
Reference rs773004449(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ITGA7
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.56088306C>T
CLNSRC
CLNACC RCV000239284.1,