Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.43 (A)
Location

Chromosome 17:66435948 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59935790

This variant has 4 HGVS names - click the plus to show

17:g.66435948A>G
ENST00000413366.7:c.206-60253A>G
ENST00000578063.5:c.206-60253A>G
ENST00000284384.6:c.198-60253A>G

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 4037 sample genotypes and is mentioned in 1 citation.

Variant displays