rs2141698
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs2141698(A;A) |
Make rs2141698(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 172425667 |
Gene | ITGA6 |
is a | snp |
is | mentioned by |
dbSNP | rs2141698 |
dbSNP (classic) | rs2141698 |
ClinGen | rs2141698 |
ebi | rs2141698 |
HLI | rs2141698 |
Exac | rs2141698 |
Gnomad | rs2141698 |
Varsome | rs2141698 |
LitVar | rs2141698 |
Map | rs2141698 |
PheGenI | rs2141698 |
Biobank | rs2141698 |
1000 genomes | rs2141698 |
hgdp | rs2141698 |
ensembl | rs2141698 |
geneview | rs2141698 |
scholar | rs2141698 |
rs2141698 | |
pharmgkb | rs2141698 |
gwascentral | rs2141698 |
openSNP | rs2141698 |
23andMe | rs2141698 |
SNPshot | rs2141698 |
SNPdbe | rs2141698 |
MSV3d | rs2141698 |
GWAS Ctlg | rs2141698 |
GMAF | 0.1465 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22148122] A missense polymorphism (rs11895564, Ala380Thr) of integrin alpha 6 is associated with the development and progression of papillary thyroid carcinoma in Korean population
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip Ancestry v2c
- On chip Ancestry v2d