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

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

dbSNP build 150 rs886041096

dbSNP: rs886041096
Position: chr1:11146756-11146756
Band: 1p36.22
Genomic Size: 1
View DNA for this feature (hg38/Human)

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

Reference allele:	A
Chimp allele:	A	Chimp strand:	-	Chimp position:	chr1:10605685-10605685
Orangutan allele:	A	Orangutan strand:	+	Orangutan position:	chr1:219201461-219201461
Macaque allele:	A	Macaque strand:	-	Macaque position:	chr1:10415096-10415096

Class	single
Validation	unknown
Function	intron_variant, nc_transcript_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: