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rs730880295

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880295(C;C)
Make rs730880295(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position43883879
GeneLACC1
is asnp
is mentioned by
dbSNPrs730880295
ebirs730880295
HLIrs730880295
Exacrs730880295
Varsomers730880295
Maprs730880295
PheGenIrs730880295
hapmaprs730880295
1000 genomesrs730880295
hgdprs730880295
ensemblrs730880295
gopubmedrs730880295
geneviewrs730880295
scholarrs730880295
googlers730880295
pharmgkbrs730880295
gwascentralrs730880295
openSNPrs730880295
23andMers730880295
23andMe allrs730880295
SNP Nexus

SNPshotrs730880295
SNPdbers730880295
MSV3drs730880295
GWAS Ctlgrs730880295
Max Magnitude0
ClinVar
Risk rs730880295(C;C)
Alt rs730880295(C;C)
Reference rs730880295(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LACC1
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.44458015T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000157633.4, RCV000171123.1,