Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.24 (A)
Location

Chromosome 16:89689495 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386569965, rs57123318

HGVS names

This variant has 18 HGVS names - Hide

16:g.89689495A>G
ENST00000512912.5:c.*105-1058A>G
ENST00000472018.5:n.171+171A>G
ENST00000504473.5:n.364-1058A>G
ENST00000503560.1:n.457+171A>G
ENST00000505733.5:n.181+171A>G
ENST00000502547.5:c.*177+171A>G
ENST00000511415.5:c.*51+171A>G
ENST00000564192.5:c.-54+171A>G
ENST00000510811.6:c.88-1058A>G
ENST00000508723.5:c.*220+171A>G
ENST00000507205.5:n.123+189A>G
ENST00000625631.1:c.88-1058A>G
ENST00000505473.5:c.-54+171A>G
ENST00000378277.8:n.86-1058A>G
ENST00000331006.12:c.20-1058A>G
ENST00000353379.11:c.160+171A>G
ENST00000514965.5:n.332+171A>G

Genotyping chips

This variant has assays on 15 chips - Show

About this variant

This variant overlaps 24 transcripts, has 4000 sample genotypes, is associated with 4 phenotypes and is mentioned in 12 citations.

Variant displays