rs1856161
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs1856161(C;T) |
Make rs1856161(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 209785823 |
Gene | C1orf74, IRF6 |
is a | snp |
is | mentioned by |
dbSNP | rs1856161 |
dbSNP (classic) | rs1856161 |
ClinGen | rs1856161 |
ebi | rs1856161 |
HLI | rs1856161 |
Exac | rs1856161 |
Gnomad | rs1856161 |
Varsome | rs1856161 |
LitVar | rs1856161 |
Map | rs1856161 |
PheGenI | rs1856161 |
Biobank | rs1856161 |
1000 genomes | rs1856161 |
hgdp | rs1856161 |
ensembl | rs1856161 |
geneview | rs1856161 |
scholar | rs1856161 |
rs1856161 | |
pharmgkb | rs1856161 |
gwascentral | rs1856161 |
openSNP | rs1856161 |
23andMe | rs1856161 |
SNPshot | rs1856161 |
SNPdbe | rs1856161 |
MSV3d | rs1856161 |
GWAS Ctlg | rs1856161 |
GMAF | 0.1377 |
Max Magnitude | 0 |
[PMID 19536891] The association between interferon regulatory factor 6 (IRF6) and nonsyndromic cleft lip with or without cleft palate in a Honduran population
ClinVar | |
---|---|
Risk | rs1856161(T;T) |
Alt | rs1856161(T;T) |
Reference | Rs1856161(C;C) |
Significance | Non-pathogenic |
Disease | Popliteal pterygium syndrome Cleft Lip +/- Cleft Palate Van der Woude syndrome |
Variation | info |
Gene | C1orf74 IRF6 |
CLNDBN | Popliteal pterygium syndrome Cleft Lip +/- Cleft Palate, Autosomal Dominant Van der Woude syndrome |
Reversed | 0 |
HGVS | NC_000001.10:g.209959168C>T |
CLNSRC | |
CLNACC | RCV000260956.1, RCV000315623.1, RCV000379584.1, |