Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

-/C|MAF: 0.36 (C)

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

Most severe consequence
Intron variant
Evidence status

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