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rs727504170

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504170(A;T)
Make rs727504170(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position38322262
GeneSPRED1
is asnp
is mentioned by
dbSNPrs727504170
ebirs727504170
HLIrs727504170
Exacrs727504170
Varsomers727504170
Maprs727504170
PheGenIrs727504170
hapmaprs727504170
1000 genomesrs727504170
hgdprs727504170
ensemblrs727504170
gopubmedrs727504170
geneviewrs727504170
scholarrs727504170
googlers727504170
pharmgkbrs727504170
gwascentralrs727504170
openSNPrs727504170
23andMers727504170
23andMe allrs727504170
SNP Nexus

SNPshotrs727504170
SNPdbers727504170
MSV3drs727504170
GWAS Ctlgrs727504170
Max Magnitude0
ClinVar
Risk rs727504170(T;T)
Alt rs727504170(T;T)
Reference rs727504170(A;A)
Significance Pathogenic
Disease not provided Autosomal dominant inheritance
Variation info
Gene SPRED1
CLNDBN not provided Autosomal dominant inheritance
Reversed 0
HGVS NC_000015.9:g.38614463A>T
CLNSRC
CLNACC RCV000153991.2, RCV000177408.1,