Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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
Evidence status

Synonyms

Archive dbSNP rs58023101

This variation has 8 HGVS names - click the plus to show

17:g.65541780T>C
ENST00000618960.2:c.957-223A>G
ENST00000375702.5:c.957-223A>G
ENST00000307078.7: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

This variation has assays on 4 chips - click the plus to show

Variation displays