Original source

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

Alleles
-/T | MAF: 0.47 (-)
Location

Chromosome 10: between 112951913 and 112951914 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs377427223, rs143225562

This variation has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 2505 individual genotypes.

Variation displays