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rs1063635

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1063635(A;A)
Make rs1063635(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31412154
GeneMICA
is asnp
is mentioned by
dbSNPrs1063635
dbSNP (classic)rs1063635
ClinGenrs1063635
ebirs1063635
HLIrs1063635
Exacrs1063635
Gnomadrs1063635
Varsomers1063635
LitVarrs1063635
Maprs1063635
PheGenIrs1063635
Biobankrs1063635
1000 genomesrs1063635
hgdprs1063635
ensemblrs1063635
geneviewrs1063635
scholarrs1063635
googlers1063635
pharmgkbrs1063635
gwascentralrs1063635
openSNPrs1063635
23andMers1063635
SNPshotrs1063635
SNPdbers1063635
MSV3drs1063635
GWAS Ctlgrs1063635
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21653640]
Trait
Title Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways.
Risk Allele
P-val 1E-17
Odds Ratio 1.3500 [1.27-1.45]


[PMID 20018019OA-icon.png] Two-stage joint selection method to identify candidate markers from genome-wide association studies.


[PMID 20041220OA-icon.png] Autoimmune disease classification by inverse association with SNP alleles.



ClinVar
Risk rs1063635(A;A)
Alt rs1063635(A;A)
Reference Rs1063635(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene MICA
CLNDBN not specified
Reversed 0
HGVS NC_000006.11:g.31379931G>A
CLNSRC
CLNACC RCV000455790.1,