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rs587776568

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776568(-;-)
Make rs587776568(-;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position5562982
GeneEVC2
is asnp
is mentioned by
dbSNPrs587776568
ebirs587776568
HLIrs587776568
Exacrs587776568
Varsomers587776568
Maprs587776568
PheGenIrs587776568
hapmaprs587776568
1000 genomesrs587776568
hgdprs587776568
ensemblrs587776568
gopubmedrs587776568
geneviewrs587776568
scholarrs587776568
googlers587776568
pharmgkbrs587776568
gwascentralrs587776568
openSNPrs587776568
23andMers587776568
23andMe allrs587776568
SNP Nexus

SNPshotrs587776568
SNPdbers587776568
MSV3drs587776568
GWAS Ctlgrs587776568
Max Magnitude0
ClinVar
Risk rs587776568(;)
Alt rs587776568(;)
Reference rs587776568(G;G)
Significance Pathogenic
Disease Curry-Hall syndrome
Variation info
Gene EVC2
CLNDBN Curry-Hall syndrome
Reversed 0
HGVS NC_000004.11:g.5564709delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000003555.3,