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rs200402328

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200402328(C;T)
Make rs200402328(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position55694442
GeneITGA7
is asnp
is mentioned by
dbSNPrs200402328
ebirs200402328
HLIrs200402328
Exacrs200402328
Varsomers200402328
Maprs200402328
PheGenIrs200402328
hapmaprs200402328
1000 genomesrs200402328
hgdprs200402328
ensemblrs200402328
gopubmedrs200402328
geneviewrs200402328
scholarrs200402328
googlers200402328
pharmgkbrs200402328
gwascentralrs200402328
openSNPrs200402328
23andMers200402328
23andMe allrs200402328
SNP Nexus

SNPshotrs200402328
SNPdbers200402328
MSV3drs200402328
GWAS Ctlgrs200402328
Max Magnitude0
ClinVar
Risk rs200402328(T;T)
Alt rs200402328(T;T)
Reference rs200402328(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ITGA7
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.56088226C>T
CLNSRC
CLNACC RCV000149980.2,