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rs587784444

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784444(C;T)
Make rs587784444(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position30738033
GeneSRCAP
is asnp
is mentioned by
dbSNPrs587784444
ebirs587784444
HLIrs587784444
Exacrs587784444
Varsomers587784444
Maprs587784444
PheGenIrs587784444
hapmaprs587784444
1000 genomesrs587784444
hgdprs587784444
ensemblrs587784444
gopubmedrs587784444
geneviewrs587784444
scholarrs587784444
googlers587784444
pharmgkbrs587784444
gwascentralrs587784444
openSNPrs587784444
23andMers587784444
23andMe allrs587784444
SNP Nexus

SNPshotrs587784444
SNPdbers587784444
MSV3drs587784444
GWAS Ctlgrs587784444
Max Magnitude0
ClinVar
Risk rs587784444(T;T)
Alt rs587784444(T;T)
Reference rs587784444(C;C)
Significance Pathogenic
Disease Floating-Harbor syndrome
Variation info
Gene SRCAP
CLNDBN Floating-Harbor syndrome
Reversed 0
HGVS NC_000016.9:g.30749354C>T
CLNSRC
CLNACC RCV000147668.1,