Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.49 (C)
Location

Chromosome 6:96111973 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57670559

HGVS names

This variant has 2 HGVS names - Hide

6:g.96111973C>T
ENST00000302103.5:c.-97-2066C>T

About this variant

This variant overlaps 1 transcript, has 2776 sample genotypes and is mentioned in 2 citations.

Variant displays