Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.47 (C)
Location

Chromosome 17:65541780 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58023101

HGVS names

This variant has 8 HGVS names - Hide

17:g.65541780T>C
ENST00000618960.4:c.957-223A>G
ENST00000375702.5:c.957-223A>G
ENST00000307078.9:c.957-223A>G
ENST00000611991.1:c.397-13080A>G
ENST00000577662.1:c.*1133-223A>G
LRG_296:g.24843A>G
LRG_296t1:c.957-223A>G

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 6 transcripts, has 4237 sample genotypes and is mentioned in 3 citations.

Variant displays