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rs775440641

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs775440641(C;C)
Make rs775440641(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position17188342
GeneCECR1
is asnp
is mentioned by
dbSNPrs775440641
ebirs775440641
HLIrs775440641
Exacrs775440641
Varsomers775440641
Maprs775440641
PheGenIrs775440641
hapmaprs775440641
1000 genomesrs775440641
hgdprs775440641
ensemblrs775440641
gopubmedrs775440641
geneviewrs775440641
scholarrs775440641
googlers775440641
pharmgkbrs775440641
gwascentralrs775440641
openSNPrs775440641
23andMers775440641
23andMe allrs775440641
SNP Nexus

SNPshotrs775440641
SNPdbers775440641
MSV3drs775440641
GWAS Ctlgrs775440641
Max Magnitude0
ClinVar
Risk rs775440641(C;C)
Alt rs775440641(C;C)
Reference rs775440641(T;T)
Significance Pathogenic
Disease Idiopathic livedo reticularis with systemic involvement
Variation info
Gene CECR1
CLNDBN Idiopathic livedo reticularis with systemic involvement
Reversed 0
HGVS NC_000022.10:g.17669232T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000169758.4,