Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.01 (A)
Location

Chromosome 19:11377110 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs318716, rs642644, rs397184

HGVS name

19:g.11377110C>A

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 3173 sample genotypes.

Variant displays