Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.43 (C)
Location

Chromosome 4:88965146 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61274991, rs17765978

This variation has 6 HGVS names - click the plus to show

4:g.88965146C>T
ENST00000511976.4:c.-22-26905G>A
ENST00000509094.4:c.605+25827G>A
ENST00000512339.4:c.428-26905G>A
ENST00000264344.8:c.605+25827G>A
ENST00000502459.4:n.1063+25827G>A

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 2361 individual genotypes and is mentioned in 4 citations.

Variation displays