Original source

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

G/- | Ancestral: G

Chromosome 9:37422884 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs371975447, rs145029881

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 8 transcripts, 1 regulatory feature, has 2504 sample genotypes and is mentioned in 1 citation.

Variant displays