Original source

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

Alleles
G/C|Ambiguity code: S
Location

Chromosome 14:73184195 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs1309160, rs1103234

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 7 transcripts.

Variant displays