Simple Nucleotide Polymorphisms (dbSNP 150) Flagged by dbSNP as Clinically Assoc

JavaScript is disabled in your web browser

You must have JavaScript enabled in your web browser to use the Genome Browser

Simple Nucleotide Polymorphisms (dbSNP 150) Flagged by dbSNP as Clinically Assoc

dbSNP build 150 rs878855328

dbSNP: rs878855328
Position: chr1:11117039-11117039
Band: 1p36.22
Genomic Size: 1
View DNA for this feature (hg38/Human)

Summary: G>A/G (chimp allele displayed first, then '>', then human alleles)
Strand: -
Observed: A/G

Reference allele:	G
Chimp allele:	G	Chimp strand:	-	Chimp position:	chr1:10575765-10575765
Orangutan allele:	G	Orangutan strand:	+	Orangutan position:	chr1:219232129-219232129
Macaque allele:	G	Macaque strand:	-	Macaque position:	chr1:10386006-10386006

Class	single
Validation	unknown
Function	intron_variant, missense_variant
Molecule Type	genomic
Weight	1
Submitter Handles	CLINVAR

Miscellaneous properties annotated by dbSNP:
SNP is in OMIM/OMIA and/or at least one submitter is a Locus-Specific Database ("clinically associated")
SNP was submitted by Locus-Specific Database

Coding annotations by dbSNP: