Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, has 2554 sample genotypes and is mentioned in 1 citation.

Variant displays