SNP Links for Gene (Select 729967) - SNP

Links from Gene

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Select item 14908132211.

rs1490813221 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:38880777 (GRCh38)
2:39107918 (GRCh37)
Canonical SPDI:: NC_000002.12:38880776:C:T
Gene:: MORN2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000002.12:g.38880777C>T, NC_000002.11:g.39107918C>T

Select item 14902636592.

rs1490263659 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 2:38874224 (GRCh38)
2:39101366 (GRCh37)
Canonical SPDI:: NC_000002.12:38874223:T:A
Gene:: DHX57 (Varview), MORN2 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.38874224T>A, NC_000002.11:g.39101366T>A

Select item 14898499043.

rs1489849904 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:38879097 (GRCh38)
2:39106238 (GRCh37)
Canonical SPDI:: NC_000002.12:38879096:G:T
Gene:: MORN2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.38879097G>T, NC_000002.11:g.39106238G>T

Select item 14898127994.

rs1489812799 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 2:38874174 (GRCh38)
2:39101316 (GRCh37)
Canonical SPDI:: NC_000002.12:38874173:C:G
Gene:: DHX57 (Varview), MORN2 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000019/5 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000002.12:g.38874174C>G, NC_000002.11:g.39101316C>G

Select item 14896901645.

rs1489690164 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 2:38875290 (GRCh38)
2:39102432 (GRCh37)
Canonical SPDI:: NC_000002.12:38875289:C:A,NC_000002.12:38875289:C:G
Gene:: DHX57 (Varview), MORN2 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.38875290C>A, NC_000002.12:g.38875290C>G, NC_000002.11:g.39102432C>A, NC_000002.11:g.39102432C>G

Select item 14896597366.

rs1489659736 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:38875987 (GRCh38)
2:39103128 (GRCh37)
Canonical SPDI:: NC_000002.12:38875986:G:A
Gene:: DHX57 (Varview), MORN2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.38875987G>A, NC_000002.11:g.39103128G>A, NM_001145450.3:c.-66G>A, NM_001145450.2:c.-282G>A, NM_001145450.1:c.-282G>A, NM_194270.1:c.-282G>A

Select item 14896157107.

rs1489615710 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 2:38878199 (GRCh38)
2:39105340 (GRCh37)
Canonical SPDI:: NC_000002.12:38878198:C:A
Gene:: MORN2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.38878199C>A, NC_000002.11:g.39105340C>A

Select item 14895471258.

rs1489547125 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:38878654 (GRCh38)
2:39105795 (GRCh37)
Canonical SPDI:: NC_000002.12:38878653:T:C
Gene:: MORN2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: C=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.38878654T>C, NC_000002.11:g.39105795T>C

Select item 14894793619.

rs1489479361 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:38877906 (GRCh38)
2:39105047 (GRCh37)
Canonical SPDI:: NC_000002.12:38877905:C:T
Gene:: DHX57 (Varview), MORN2 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.38877906C>T, NC_000002.11:g.39105047C>T

Select item 148898414710.

rs1488984147 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 2:38878618 (GRCh38)
2:39105759 (GRCh37)
Canonical SPDI:: NC_000002.12:38878617:G:A,NC_000002.12:38878617:G:T
Gene:: MORN2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.38878618G>A, NC_000002.12:g.38878618G>T, NC_000002.11:g.39105759G>A, NC_000002.11:g.39105759G>T

Select item 148894320311.

rs1488943203 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:38881204 (GRCh38)
2:39108345 (GRCh37)
Canonical SPDI:: NC_000002.12:38881203:A:G
Gene:: MORN2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.38881204A>G, NC_000002.11:g.39108345A>G

Select item 148891564412.

rs1488915644 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 2:38882073 (GRCh38)
2:39109214 (GRCh37)
Canonical SPDI:: NC_000002.12:38882072:T:G
Gene:: MORN2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.38882073T>G, NC_000002.11:g.39109214T>G

Select item 148809951613.

rs1488099516 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 2:38882724 (GRCh38)
2:39109865 (GRCh37)
Canonical SPDI:: NC_000002.12:38882723:T:A
Gene:: MORN2 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.38882724T>A, NC_000002.11:g.39109865T>A

Select item 148784638114.

rs1487846381 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:38877589 (GRCh38)
2:39104730 (GRCh37)
Canonical SPDI:: NC_000002.12:38877588:A:C
Gene:: DHX57 (Varview), MORN2 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.38877589A>C, NC_000002.11:g.39104730A>C

Select item 148762440115.

rs1487624401 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:38877919 (GRCh38)
2:39105060 (GRCh37)
Canonical SPDI:: NC_000002.12:38877918:C:T
Gene:: DHX57 (Varview), MORN2 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000002.12:g.38877919C>T, NC_000002.11:g.39105060C>T

Select item 148761392016.

rs1487613920 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:38882407 (GRCh38)
2:39109548 (GRCh37)
Canonical SPDI:: NC_000002.12:38882406:T:C
Gene:: MORN2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000043/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000013/2 (GnomAD_exomes)
C=0.000106/2 (TOMMO)
HGVS:: NC_000002.12:g.38882407T>C, NC_000002.11:g.39109548T>C

Select item 148744392917.

rs1487443929 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 2:38876062 (GRCh38)
2:39103203 (GRCh37)
Canonical SPDI:: NC_000002.12:38876061:C:A,NC_000002.12:38876061:C:G
Gene:: DHX57 (Varview), MORN2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.38876062C>A, NC_000002.12:g.38876062C>G, NC_000002.11:g.39103203C>A, NC_000002.11:g.39103203C>G, NM_001145450.3:c.10C>A, NM_001145450.3:c.10C>G, NM_001145450.2:c.-207C>A, NM_001145450.2:c.-207C>G, NM_001145450.1:c.-207C>A, NM_001145450.1:c.-207C>G, NM_194270.1:c.-207C>A, NM_194270.1:c.-207C>G, NP_001138922.2:p.Gln4Lys, NP_001138922.2:p.Gln4Glu

Select item 148676759518.

rs1486767595 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 2:38874396 (GRCh38)
2:39101538 (GRCh37)
Canonical SPDI:: NC_000002.12:38874395:A:C,NC_000002.12:38874395:A:G
Gene:: DHX57 (Varview), MORN2 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant,genic_upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: C=0.0051/15 (KOREAN)
HGVS:: NC_000002.12:g.38874396A>C, NC_000002.12:g.38874396A>G, NC_000002.11:g.39101538A>C, NC_000002.11:g.39101538A>G

Select item 148655252919.

rs1486552529 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:38876229 (GRCh38)
2:39103370 (GRCh37)
Canonical SPDI:: NC_000002.12:38876228:A:C
Gene:: DHX57 (Varview), MORN2 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.38876229A>C, NC_000002.11:g.39103370A>C

Select item 148633328720.

rs1486333287 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 2:38883023 (GRCh38)
2:39110164 (GRCh37)
Canonical SPDI:: NC_000002.12:38883022:T:C,NC_000002.12:38883022:T:G
Gene:: MORN2 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000015/4 (TOPMED)
C=0.000035/1 (TOMMO)
HGVS:: NC_000002.12:g.38883023T>C, NC_000002.12:g.38883023T>G, NC_000002.11:g.39110164T>C, NC_000002.11:g.39110164T>G

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