Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/C | MAF: 0.36 (C)
Location

Chromosome 5: between 159316222 and 159316223 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2549 sample genotypes and is mentioned in 1 citation.

Variant displays