Original source

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

Alleles
-/T
Location

Chromosome 14: between 92096911 and 92096912 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs71123315

This variation has 50 HGVS names - click the plus to show

About this variant

This variant overlaps 51 transcripts and has 2 individual genotypes.

Variation displays