Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 3:47657937 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs7372942

HGVS names

This variant has 3 HGVS names - Hide

3:g.47657937C>T
ENST00000425518.5:n.2210+3357G>A
ENST00000254480.9:c.2320+3357G>A

About this variant

This variant overlaps 2 transcripts and has 2 sample genotypes.

Variant displays